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Efficacy of Ramelteon on Speeding Up Sleep in Subjects With Delayed Sleep Phase Syndrome

Primary Purpose

Sleep Disorders, Circadian Rhythm

Status

Completed

Phase

Phase 2

Locations

United States

Study Type

Interventional

Intervention

Ramelteon

Placebo

About this trial

This is an interventional treatment trial for Sleep Disorders, Circadian Rhythm focused on measuring Delayed sleep phase syndrome; drug therapy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Females of childbearing potential who is sexually active must agree to use adequate contraception from screening throughout the duration of the study.
Must have a diagnosis of Delayed Sleep Phase Syndrome according to International Classification of Sleep Disorders criteria for at least 3 months.
Based on sleep history, subject's habitual sleep time is more than 3 hours later than the desired sleep time.
Must have had self reported insomnia which is defined per the sleep history as his or her sleep latency of at least 45 minutes when attempting to sleep at desired sleep time required by his or her work or school schedule.
The subjective sleep latency via Post sleep questionnaire during outpatient screening period must be greater than or equal to 45 minutes during every working night or school night provided the subject went to bed at their desired sleep time.
During single blind placebo run-in Polysomnography screening nights, subject is instructed to go to bed at their desired bed time and must demonstrate difficulty in falling asleep based on the following criteria:
- During Polysomnography screening nights when the subject goes to bed at their desired sleep time or
- The average of total wake time
Is in good health as determined by a medical and psychiatric history, physical examination, Electrocardiogram, and serum chemistry and hematology.
Is able to complete self-rating scales via interactive voice response system, and has a touch tone phone.
Is willing to comply with study procedures and restrictions with fixed sleep time and wake time during the study and to attend regularly scheduled clinic visits as specified in this protocol.
Has a body mass index is between 18 and 34 kg/m2, inclusive.
Has a negative urine test result for selected substances of abuse (including alcohol).
Has a negative test result for hepatitis B surface antigen and hepatitis C virus antibody or history of human immunodeficiency virus.
Has not used pharmacological sleep assistance for more than 4 times/week during the 3 months prior to Initial Screening.
Must have discontinued use of all pharmacological sleep aids beginning 1 week prior to Visit 2 and for the duration of the trial.

Exclusion Criteria:

Has a known hypersensitivity to ramelteon or related compounds, including melatonin and melatonin-related compounds or 5-hydroxytryptophan.
Has participated in any other investigational study and/or taken any investigational drug within 30 days or 5 half-lives prior to the first dose of study medication, whichever is longer.
Has flown across greater than 3 time zones within the past 3 months prior to administration of study medication.
Has sleep schedule changes required by employment (eg, shift worker) within 3 months prior to the administration of study medication.
Has participated in a weight loss program or has substantially altered their exercise routine within 30 days prior to the administration of study medication.
Has a history of alcohol abuse within the past 12 months, as defined in the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision, or regularly consumes more than 14 alcoholic drinks per week or consumes any alcoholic drinks within 24 hours of Screening Visit.
Has a history of drug abuse within the past 12 months.
Has a current, clinically significant neurological (including cognitive), hepatic, renal, endocrine, cardiovascular, gastrointestinal, pulmonary, hematological, or metabolic disease, as determined by the investigator.
Has a probable current diagnosis of another circadian rhythm disorder or a sleep disorder other than Delayed Sleep Phase Syndrome that is the primary cause of insomnia.
Had an apnea hypopnea index greater than 10 on the first night of Polysomnography Screening.
Has periodic limb movements during sleep with arousal index greater than 10 as seen on the first night of Polysomnography screening only.
Has a positive urine drug screen or breathalyzer test.
Has ever had a history of seizures; sleep apnea, restless leg syndrome, chronic obstructive pulmonary disease, fibromyalgia, or a positive test result for the aforementioned ailments on the screening Polysomnography, schizophrenia, bipolar disorder, mental retardation, or cognitive disorder.
Has a history of psychiatric disorder (including anxiety or depression) within the past 12 months.
Smokes more than 3 cigarettes per day or uses tobacco products during nightly awakenings.
Routinely consumes caffeine including coffee, tea and/or other caffeine-containing beverages or food averaging more than 600 mg of caffeine per day.
Has used any central nervous system drug or other medications, including those used to treat psychiatric disorders, known to affect sleep/wake function within 1 week whichever is longer prior to the administration of single blind study drug.
Used melatonin, or other drugs/supplements known to affect sleep/wake function within 1 week (or 5 half lives of the drug) whichever is longer prior to the first dose of single blind medication.
Is required to take or intends to continue taking any disallowed medication, any prescription medication, herbal treatment or over-the counter medication that may interfere with evaluation of the study medication, including:
- Anxiolytics
- Hypnotics
- Antidepressants
- Anticonvulsants
- Sedating H1 antihistamines
- Systemic steroids
- Respiratory stimulants
- Decongestants
- Antipsychotics
- Muscle relaxants
- Over-the-counter and prescription diet aids
- Narcotic analgesics
- Beta Blockers
- St. John's wort
- Kava kava
- Ginkgo biloba
- Modafinil
- Coumadin
- Heparin
- Melatonin and all other drugs or supplements known to affect sleep/wake function will be prohibited within 1 week of the first dose of study medication and during the entire study.
Has any clinically important abnormal finding as determined by a medical history, physical examination, Electrocardiogram, or clinical laboratory tests as determined by the investigator.
Has a positive hepatitis panel including anti- Hepatitis A Virus, hepatitis B surface antigen or anti- hepatitis C virus.
Has any additional condition(s) that in the investigator's opinion would:
- Affect sleep/wake function
- Prohibit the subject from completing the study, or
- Not be in the best interest of the subject.
Exhibits a placebo response during single-blinded placebo run in period.
Individuals with a habitual sleep time later than 4:00 am should not be included in the study.

Sites / Locations

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Placebo Comparator

Arm Label

Ramelteon 1 mg QD

Ramelteon 4 mg QD

Ramelteon 8 mg QD

Placebo QD

Arm Description

Outcomes

Primary Outcome Measures

Latency to Persistent Sleep Over a 2-night Average Measured by Polysomnography (Nights 6-7)

The elapsed time from the beginning of the polysomnography recording to the onset of the first 10 minutes of continuous sleep (ie, total number of epochs before the first 20 consecutive non-wake epochs divided by 2).

Secondary Outcome Measures

Latency to Persistent Sleep Over a 2-night Average Measured by Polysomnography (Nights 13-14)

Total Sleep Time Over a 2-night Average Measured by Polysomnography (Nights 6-7)

The sum of all of the minutes of Stages 1, 2, 3, 4, and rapid eye movement (REM) sleep.

Total Sleep Time Over a 2-night Average Measured by Polysomnography (Nights 13-14)

The sum of all of the minutes of Stages 1, 2, 3, 4, and REM sleep.

Sleep Efficiency Over a 2-night Average Measured by Polysomnography (0-3 Hours) (Nights 6-7)

The total sleep time divided by time-in-bed, multiplied by 100.

Sleep Efficiency Over a 2-night Average Measured by Polysomnography (0-3 Hours) (Nights 13-14)

The total sleep time divided by time-in-bed, multiplied by 100.

Sleep Efficiency Over a 2-night Average Measured by Polysomnography (0-8 Hours) (Nights 6-7)

The total sleep time divided by time-in-bed, multiplied by 100.

Sleep Efficiency Over a 2-night Average Measured by Polysomnography (0-8 Hours) (Nights 13-14)

The total sleep time divided by time-in-bed, multiplied by 100.

Wake Time After Sleep Onset Over a 2-night Average Measured by Polysomnography (Nights 6-7)

The number of wake minutes after the onset of persistent sleep prior to the end of recording.

Wake Time After Sleep Onset Over a 2-night Average Measured by Polysomnography (Nights 13-14)

The number of wake minutes after the onset of persistent sleep prior to the end of recording.

Number of Awakenings Over a 2-night Average Measured by Polysomnography (Nights 6-7)

The number of times after onset of persistent sleep that there is a wake entry of at least 2 epochs in duration. Each entry must be separated by stage 2, stage 3/4 non-REM (NREM) sleep, or REM sleep to be counted.

Number of Awakenings Over a 2-night Average Measured by Polysomnography (Nights 13-14)

Total Wake Time Over a 2-night Average Measured by Polysomnography (Nights 6-7)

The sum of all the minutes of Stage Wake from the beginning of the recording to the end of recording.

Total Wake Time Over a 2-night Average Measured by Polysomnography (Nights 13-14)

The sum of all the minutes of Stage Wake from the beginning of the recording to the end of recording.

Sleep Time Over a 2-night Average Measured by Polysomnography (Nights 6-7)

Sleep time was measured as the clock time the subject went to sleep. Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Sleep Time Over a 2-night Average Measured by Polysomnography (Nights 13-14)

Sleep time was measured as the clock time the subject went to sleep. Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Wake Time Over a 2-night Average Measured by Polysomnography (Nights 6-7)

Wake Time was measured as the clock time that the subject got up in the morning. Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Wake Time Over a 2-night Average Measured by Polysomnography (Nights 13-14)

Wake Time was measured as the clock time that the subject got up in the morning. Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Total Sleep Time Measured by Actigraphy (Nights 6-7)

Total sleep time calculated using the total number of epochs (number of movements recorded by actigraphy watch worn by subject) that are less than or equal to 40, measured between the start time and end time during the nocturnal sleep interval, scored as SLEEP by the actigraphy software.

Total Sleep Time Measured by Actigraphy (Nights 13-14)

Total sleep time pertains to the total number of epochs (number of movements recorded by actigraphy watch worn by subject) that are less than or equal to 40, measured between the start time and end time during the nocturnal sleep interval, scored as SLEEP by the actigraphy software.

Sleep Efficiency Measured by Actigraphy (Nights 6-7)

Sleep efficiency pertains to the scored total sleep time (recorded by actigraphy watch worn by subject) of the sleep interval divided by total time in bed minus total invalid time (Sleep/Wake), multiplied by 100.

Sleep Efficiency Measured by Actigraphy (Nights 13-14)

Wake Time During Sleep Interval Measured by Actigraphy (Nights 6-7)

Wake time during sleep is the total number of epochs (number of movements recorded by actigraphy watch worn by subject) between the start time and the end time of the given sleep interval, scored as WAKE by the software (or manually set as WAKE by the practitioner using the software), multiplied by the Epoch length in minutes.

Wake Time During Sleep Interval Measured by Actigraphy (Nights 13-14)

Wake Bouts Measured by Actigraphy (Nights 6-7)

The number of wake bouts pertains to the total number of continuous blocks (recorded by actigraphy watch worn by subject), with one or more epochs in duration, and with each epoch of each clock scored as WAKE between the start time and the end time of the given interval.

Wake Bouts Measured by Actigraphy (Nights 13-14)

Sleep Latency Measured by Actigraphy (Nights 6-7)

The elapsed time from the beginning of the recording to the onset of the first 10 minutes of continuous sleep (recorded by actigraphy watch worn by subject).

Sleep Latency Measured by Actigraphy (Nights 13-14)

The elapsed time from the beginning of the recording to the onset of the first 10 minutes of continuous sleep (recorded by actigraphy watch worn by subject).

Sleep Time Measured by Actigraphy (Nights 6-7)

Clock time subject goes to sleep (recorded by actigraphy watch worn by subject). Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Sleep Time Measured by Actigraphy (Nights 13-14)

Clock time subject goes to sleep (recorded by actigraphy watch worn by subject). Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Wake Time Measured by Actigraphy (Nights 6-7)

Clock time subject wakes up (recorded by actigraphy watch worn by subject). Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Wake Time Measured by Actigraphy (Nights 13-14)

Clock time subject wakes up (recorded by actigraphy watch worn by subject). Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Subjective Sleep Latency Measured by a Post-sleep Questionnaire (Nights 6-7)

Subjective sleep latency was an average of 2 nights responses and measured by post-sleep questionnaire in response to the question, "How long do you think it took you to fall asleep last night?"

Subjective Sleep Latency Measured by a Post-sleep Questionnaire (Nights 13-14)

Subjective sleep latency was an average of 2 nights responses and measured by post-sleep questionnaire in response to the question, "How long do you think it took you to fall asleep last night?"

Subjective Total Sleep Time Measured by a Post-sleep Questionnaire (Nights 6-7)

Subjective total sleep time was an average of 2 nights responses and measured by post-sleep questionnaire in response to the question, "How long (total hours and minutes) do you think you slept last night?"

Subjective Total Sleep Time Measured by a Post-sleep Questionnaire (Nights 13-14)

Subjective Wake Time After Sleep Onset Measured by a Post-sleep Questionnaire (Nights 6-7)

Subjective wake time after sleep onset was an average of 2 nights responses and measured by post-sleep questionnaire in response to the question, "Did you wake up during the night? If "yes", what is the total time you think you were awake?"

Subjective Wake Time After Sleep Onset Measured by a Post-sleep Questionnaire (Nights 13-14)

Subjective Number of Awakenings Measured by a Post-sleep Questionnaire (Nights 6-7)

Subjective number of awakenings was an average of 2 nights responses and measured by post-sleep questionnaire in response to the question, "Did you wake up during the night? If "yes", how many times do you think you woke up?"

Subjective Number of Awakenings Measured by a Post-sleep Questionnaire (Nights 13-14)

Subjective Sleep Quality Measured by a Post-sleep Questionnaire (Nights 6-7)

Subjective sleep quality was an average of 2 nights responses and measured by post-sleep questionnaire in response to the question, "How would you describe the quality of your sleep last night?" Scores were based on the following scale: Extremely Poor=7; Very Poor=6; Poor=5; Fair=4; Good=3; Very Good=2; Excellent=1.

Subjective Sleep Quality Measured by a Post-sleep Questionnaire (Nights 13-14)

Subjective Sleep Time Measured by a Post-sleep Questionnaire (Nights 6-7)

Subjective sleep time was an average of 2 nights responses and measured by post-sleep questionnaire in response to the question, "What time did you try to go to sleep last night?" Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Subjective Sleep Time Measured by a Post-sleep Questionnaire (Nights 13-14)

Subjective Getting up in the Morning Measured by a Post-sleep Questionnaire (Nights 6-7)

The score was an average of 2 nights responses. If subjects had a work or school day, the answer to, "How easy was it for you to wake or get up in the morning when on a school or working night?" was based on the following scale: Extremely Difficult =7; Very Difficult =6; Difficult =5; Neither =4; Easy =3; Very Easy =2; Extremely Easy =1.

Subjective Getting up in the Morning Measured by a Post-sleep Questionnaire (Nights 13-14)

Subjective Ability to Concentrate in the Morning Measured by a Post-sleep Questionnaire (Nights 6-7)

Subjective ability to concentrate was an average of 2 nights responses and measured by post-sleep questionnaire in response to the question, "How would you describe your ability to concentrate this morning?" Scores were based on the following scale: Extremely Poor=7; Very Poor=6; Poor=5; Fair=4; Good=3; Very Good=2; Excellent=1.

Subjective Ability to Concentrate in the Morning Measured by a Post-sleep Questionnaire (Nights 13-14)

Subjective Level of Alertness Measured by a Post-sleep Questionnaire (Nights 6-7)

Subjective level of alertness was an average of 2 nights responses and measured by post-sleep questionnaire in response to the question, "How would you describe your level of alertness this morning?" Scores were based on the following scale: Extremely Poor=7; Very Poor=6; Poor=5; Fair=4; Good=3; Very Good=2; Excellent=1.

Subjective Level of Alertness Measured by a Post-sleep Questionnaire (Nights 13-14)

Next Morning Residual Effects Assessments of Psychomotor and Cognitive Function Via Digit Symbol Substitution Test

The number of correct digit-for-number substitutions on a Digit Symbol Substitution Test in the 90-second period was recorded to assess psychomotor and cognitive function. The score was the average of 2 mornings' tests. Worst Value: 0. Best Value: No Limit.

Next Morning Residual Effects Assessments of Psychomotor and Cognitive Function Via Memory Recall Test--Immediate

After 16 words were read to a subject, a subject was given 2 minutes to write down as many words as he/she remembered. The correct number of words written was scored, and the average of 2 mornings' tests was calculated.

Next Morning Residual Effects Assessments of Psychomotor and Cognitive Function Via Memory Recall Test--Delayed

After 16 words were read to a subject, a subject waited 1 minute and then was given 2 minutes to write down as many words as he/she remembered. The correct number of words written was scored, and the average of 2 mornings' tests was calculated.

Visual Analogue Scale for Mood

Subjects marked visual scales (in millimeters) that represented ranges of emotions (eg, calm to anxious; normal to bloated; energetic to fatigued). Individual subject composite scores were calculated, and the average of 2 tests were analyzed. Worst Value: 0 mm. Best Value: 100 mm. The farther to the left a subject marks, the better their mood; farther to the right, the more distressed the mood. Higher numbers indicate a more distressed mood.

Visual Analogue Scale for Feelings

Subjects marked visual scales (in millimeters) that represented ranges of emotions (eg, calm to anxious; normal to bloated; energetic to fatigued). Individual subject composite scores were calculated, and the average of 2 tests were analyzed. Worst Value:0 mm.. Best Value:100 mm.. The farther to the left a subject marks, the better their mood; farther to the right, the more distressed the mood. Higher numbers indicate a more distressed mood.

The Time of Dim Light Melatonin Secretion Onset

Linear Dim Light Melatonin Secretion Onset is defined as the first time of the evening (on a 24-hour clock) when the melatonin level rises above 3.0 pg/ml with a positive slope. Units are hours and minutes on a 24-hour clock, expressed in decimal time.

The Time of Dim Light Melatonin Secretion Offset

Dim Light Melatonin Secretion Offset is defined as the first time of the morning (on a 24-hour clock) when the melatonin drops to below 3 pg/mL with a negative slope. Units are hours and minutes on a 24-hour clock, expressed in decimal time.

The Total Duration of Secretion of Melatonin

The total duration of time from Dim Light Melatonin Secretion Onset to Dim Light Melatonin Secretion Offset.

The Area Under the Concentration-time Curve of Melatonin From 0 to 24 Hours

Area under the concentration-time curve is a measure of total drug exposure.

Average Cmax (Maximum Observed Plasma Concentration) Calculated as the Average of Three Highest Cmax Observations Within the Sampling Period.

Average Cmax calculated as the average of three highest Cmax observations within the sampling period.

Full Information

NCT ID

NCT00593736

First Posted

January 2, 2008

Last Updated

February 27, 2012

Sponsor

Takeda

1. Study Identification

Unique Protocol Identification Number

NCT00593736

Brief Title

Efficacy of Ramelteon on Speeding Up Sleep in Subjects With Delayed Sleep Phase Syndrome

Official Title

A Randomized, Double-Blind, Placebo-Controlled, Parallel, Proof of Concept Study to Evaluate the Effectiveness of Ramelteon to Advance the Timing of Sleep in Individuals With Delayed Sleep Phase Syndrome (DSPS)

Study Type

Interventional

2. Study Status

Record Verification Date

February 2012

Overall Recruitment Status

Completed

Study Start Date

October 2007 (undefined)

Primary Completion Date

May 2008 (Actual)

Study Completion Date

May 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor

Name of the Sponsor

Takeda

4. Oversight

Data Monitoring Committee

5. Study Description

Brief Summary

The purpose of this study is to evaluate the ability of ramelteon, once daily (QD), to advance the timing of sleep in individuals with delayed sleep phase syndrome.

Detailed Description

Delayed sleep phase syndrome is the most common circadian disorder in adolescents and most adults with the condition report onset of symptoms during childhood or adolescence. Delayed Sleep Phase Syndrome involves a chronic mismatch between the usual daily schedule required by the individual's environment and his or her circadian sleep wake pattern. Individuals suffering from delayed Sleep Phase Syndrome experience great difficulty when attempting to fall asleep before 1-2 am, if not later, as well as rising at acceptable hours of the morning despite having completely normal sleep architecture and sleep duration. Delayed Sleep Phase Syndrome is a sleep disorder that results from a dysregulation of the circadian sleep-wake rhythm. Delayed Sleep Phase Syndrome is often the cause of severe insomnia and is associated with excessive daytime sleepiness, major depressive disorder and severe disruption of education, work and social functioning. Its major symptom is extreme difficulty initiating sleep at a conventional hour and waking on time in the morning for school or work. Ramelteon is a selective melatonin type 1 (MT1) and type 2 (MT2) receptor agonist. The purpose of this study is to evaluate the ability of ramelteon to advance the timing of sleep in individuals with delayed sleep phase syndrome. The effect of ramelteon will be analyzed based on collection of information from a post-sleep questionnaire completed by participants, and data collected by polysomnography in a sleep clinic setting. Total participation time involved in this study will be approximately 7 weeks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Sleep Disorders, Circadian Rhythm

Keywords

Delayed sleep phase syndrome; drug therapy

7. Study Design

Primary Purpose

Treatment

Study Phase

Phase 2

Interventional Study Model

Parallel Assignment

Masking

ParticipantInvestigator

Allocation

Randomized

Enrollment

132 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Ramelteon 1 mg QD

Arm Type

Experimental

Arm Title

Ramelteon 4 mg QD

Arm Type

Experimental

Arm Title

Ramelteon 8 mg QD

Arm Type

Experimental

Arm Title

Placebo QD

Arm Type

Placebo Comparator

Intervention Type

Drug

Intervention Name(s)

Ramelteon

Other Intervention Name(s)

Rozerem™, TAK-375

Intervention Description

Ramelteon 1 mg, tablets, orally, once daily for up to two weeks.

Intervention Type

Drug

Intervention Name(s)

Ramelteon

Other Intervention Name(s)

Rozerem™, TAK-375

Intervention Description

Ramelteon 4 mg, tablets, orally, once daily for up to two weeks.

Intervention Type

Drug

Intervention Name(s)

Ramelteon

Other Intervention Name(s)

Rozerem™, TAK-375

Intervention Description

Ramelteon 8 mg, tablets, orally, once daily for up to two weeks.

Intervention Type

Drug

Intervention Name(s)

Placebo

Intervention Description

Ramelteon placebo-matching tablets, orally, once daily for up to two weeks.

Primary Outcome Measure Information:

Title

Latency to Persistent Sleep Over a 2-night Average Measured by Polysomnography (Nights 6-7)

Description

Time Frame

Nights 6-7

Secondary Outcome Measure Information:

Title

Latency to Persistent Sleep Over a 2-night Average Measured by Polysomnography (Nights 13-14)

Description

Time Frame

Nights 13-14

Title

Total Sleep Time Over a 2-night Average Measured by Polysomnography (Nights 6-7)

Description

The sum of all of the minutes of Stages 1, 2, 3, 4, and rapid eye movement (REM) sleep.

Time Frame

Nights 6-7

Title

Total Sleep Time Over a 2-night Average Measured by Polysomnography (Nights 13-14)

Description

The sum of all of the minutes of Stages 1, 2, 3, 4, and REM sleep.

Time Frame

Nights 13-14

Title

Sleep Efficiency Over a 2-night Average Measured by Polysomnography (0-3 Hours) (Nights 6-7)

Description

The total sleep time divided by time-in-bed, multiplied by 100.

Time Frame

Nights 6-7

Title

Sleep Efficiency Over a 2-night Average Measured by Polysomnography (0-3 Hours) (Nights 13-14)

Description

The total sleep time divided by time-in-bed, multiplied by 100.

Time Frame

Nights 13-14

Title

Sleep Efficiency Over a 2-night Average Measured by Polysomnography (0-8 Hours) (Nights 6-7)

Description

The total sleep time divided by time-in-bed, multiplied by 100.

Time Frame

Nights 6-7

Title

Sleep Efficiency Over a 2-night Average Measured by Polysomnography (0-8 Hours) (Nights 13-14)

Description

The total sleep time divided by time-in-bed, multiplied by 100.

Time Frame

Nights 13-14

Title

Wake Time After Sleep Onset Over a 2-night Average Measured by Polysomnography (Nights 6-7)

Description

The number of wake minutes after the onset of persistent sleep prior to the end of recording.

Time Frame

Nights 6-7

Title

Wake Time After Sleep Onset Over a 2-night Average Measured by Polysomnography (Nights 13-14)

Description

The number of wake minutes after the onset of persistent sleep prior to the end of recording.

Time Frame

Nights 13-14

Title

Number of Awakenings Over a 2-night Average Measured by Polysomnography (Nights 6-7)

Description

Time Frame

Nights 6-7

Title

Number of Awakenings Over a 2-night Average Measured by Polysomnography (Nights 13-14)

Description

Time Frame

Nights 13-14

Title

Total Wake Time Over a 2-night Average Measured by Polysomnography (Nights 6-7)

Description

The sum of all the minutes of Stage Wake from the beginning of the recording to the end of recording.

Time Frame

Nights 6-7

Title

Total Wake Time Over a 2-night Average Measured by Polysomnography (Nights 13-14)

Description

The sum of all the minutes of Stage Wake from the beginning of the recording to the end of recording.

Time Frame

Nights 13-14

Title

Sleep Time Over a 2-night Average Measured by Polysomnography (Nights 6-7)

Description

Sleep time was measured as the clock time the subject went to sleep. Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Time Frame

Nights 6-7

Title

Sleep Time Over a 2-night Average Measured by Polysomnography (Nights 13-14)

Description

Sleep time was measured as the clock time the subject went to sleep. Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Time Frame

Nights 13-14

Title

Wake Time Over a 2-night Average Measured by Polysomnography (Nights 6-7)

Description

Wake Time was measured as the clock time that the subject got up in the morning. Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Time Frame

Nights 6-7

Title

Wake Time Over a 2-night Average Measured by Polysomnography (Nights 13-14)

Description

Wake Time was measured as the clock time that the subject got up in the morning. Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Time Frame

Nights 13-14

Title

Total Sleep Time Measured by Actigraphy (Nights 6-7)

Description

Time Frame

Nights 6-7

Title

Total Sleep Time Measured by Actigraphy (Nights 13-14)

Description

Time Frame

Nights 13-14

Title

Sleep Efficiency Measured by Actigraphy (Nights 6-7)

Description

Time Frame

Nights 6-7

Title

Sleep Efficiency Measured by Actigraphy (Nights 13-14)

Description

Time Frame

Nights 13-14

Title

Wake Time During Sleep Interval Measured by Actigraphy (Nights 6-7)

Description

Time Frame

Nights 6-7

Title

Wake Time During Sleep Interval Measured by Actigraphy (Nights 13-14)

Description

Time Frame

Nights 13-14

Title

Wake Bouts Measured by Actigraphy (Nights 6-7)

Description

Time Frame

Nights 6-7

Title

Wake Bouts Measured by Actigraphy (Nights 13-14)

Description

Time Frame

Nights 13-14

Title

Sleep Latency Measured by Actigraphy (Nights 6-7)

Description

The elapsed time from the beginning of the recording to the onset of the first 10 minutes of continuous sleep (recorded by actigraphy watch worn by subject).

Time Frame

Nights 6-7

Title

Sleep Latency Measured by Actigraphy (Nights 13-14)

Description

The elapsed time from the beginning of the recording to the onset of the first 10 minutes of continuous sleep (recorded by actigraphy watch worn by subject).

Time Frame

Nights 13-14

Title

Sleep Time Measured by Actigraphy (Nights 6-7)

Description

Clock time subject goes to sleep (recorded by actigraphy watch worn by subject). Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Time Frame

Nights 6-7

Title

Sleep Time Measured by Actigraphy (Nights 13-14)

Description

Clock time subject goes to sleep (recorded by actigraphy watch worn by subject). Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Time Frame

Nights 13-14

Title

Wake Time Measured by Actigraphy (Nights 6-7)

Description

Clock time subject wakes up (recorded by actigraphy watch worn by subject). Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Time Frame

Nights 6-7

Title

Wake Time Measured by Actigraphy (Nights 13-14)

Description

Clock time subject wakes up (recorded by actigraphy watch worn by subject). Units are hours and minutes on a 24-hour clock, expressed in decimal time.

Time Frame

Nights 13-14

Title

Subjective Sleep Latency Measured by a Post-sleep Questionnaire (Nights 6-7)

Description

Subjective sleep latency was an average of 2 nights responses and measured by post-sleep questionnaire in response to the question, "How long do you think it took you to fall asleep last night?"

Time Frame

Nights 6-7

Title

Subjective Sleep Latency Measured by a Post-sleep Questionnaire (Nights 13-14)

Description

Subjective sleep latency was an average of 2 nights responses and measured by post-sleep questionnaire in response to the question, "How long do you think it took you to fall asleep last night?"

Time Frame

Nights 13-14

Title

Subjective Total Sleep Time Measured by a Post-sleep Questionnaire (Nights 6-7)

Description

Time Frame

Nights 6-7

Title

Subjective Total Sleep Time Measured by a Post-sleep Questionnaire (Nights 13-14)

Description

Time Frame

Nights 13-14

Title

Subjective Wake Time After Sleep Onset Measured by a Post-sleep Questionnaire (Nights 6-7)

Description

Time Frame

Nights 6-7

Title

Subjective Wake Time After Sleep Onset Measured by a Post-sleep Questionnaire (Nights 13-14)

Description

Time Frame

Nights 13-14

Title

Subjective Number of Awakenings Measured by a Post-sleep Questionnaire (Nights 6-7)

Description

Time Frame

Nights 6-7

Title

Subjective Number of Awakenings Measured by a Post-sleep Questionnaire (Nights 13-14)

Description

Time Frame

Nights 13-14

Title

Subjective Sleep Quality Measured by a Post-sleep Questionnaire (Nights 6-7)

Description

Time Frame

Nights 6-7

Title

Subjective Sleep Quality Measured by a Post-sleep Questionnaire (Nights 13-14)

Description

Time Frame

Nights 13-14

Title

Subjective Sleep Time Measured by a Post-sleep Questionnaire (Nights 6-7)

Description

Time Frame

Nights 6-7

Title

Subjective Sleep Time Measured by a Post-sleep Questionnaire (Nights 13-14)

Description

Time Frame

Nights 13-14

Title

Subjective Getting up in the Morning Measured by a Post-sleep Questionnaire (Nights 6-7)

Description

Time Frame

Nights 6-7

Title

Subjective Getting up in the Morning Measured by a Post-sleep Questionnaire (Nights 13-14)

Description

Time Frame

Nights 13-14

Title

Subjective Ability to Concentrate in the Morning Measured by a Post-sleep Questionnaire (Nights 6-7)

Description

Time Frame

Nights 6-7

Title

Subjective Ability to Concentrate in the Morning Measured by a Post-sleep Questionnaire (Nights 13-14)

Description

Time Frame

Nights 13-14

Title

Subjective Level of Alertness Measured by a Post-sleep Questionnaire (Nights 6-7)

Description

Time Frame

Nights 6-7

Title

Subjective Level of Alertness Measured by a Post-sleep Questionnaire (Nights 13-14)

Description

Time Frame

Nights 13-14

Title

Next Morning Residual Effects Assessments of Psychomotor and Cognitive Function Via Digit Symbol Substitution Test

Description

Time Frame

Day 15

Title

Next Morning Residual Effects Assessments of Psychomotor and Cognitive Function Via Memory Recall Test--Immediate

Description

Time Frame

Day 15

Title

Next Morning Residual Effects Assessments of Psychomotor and Cognitive Function Via Memory Recall Test--Delayed

Description

Time Frame

Day 15

Title

Visual Analogue Scale for Mood

Description

Time Frame

Day 15

Title

Visual Analogue Scale for Feelings

Description

Subjects marked visual scales (in millimeters) that represented ranges of emotions (eg, calm to anxious; normal to bloated; energetic to fatigued). Individual subject composite scores were calculated, and the average of 2 tests were analyzed. Worst Value:0 mm.. Best Value:100 mm.. The farther to the left a subject marks, the better their mood; farther to the right, the more distressed the mood. Higher numbers indicate a more distressed mood.

Time Frame

Day 15

Title

The Time of Dim Light Melatonin Secretion Onset

Description

Time Frame

Day 15

Title

The Time of Dim Light Melatonin Secretion Offset

Description

Time Frame

Day 15

Title

The Total Duration of Secretion of Melatonin

Description

The total duration of time from Dim Light Melatonin Secretion Onset to Dim Light Melatonin Secretion Offset.

Time Frame

Day 15

Title

The Area Under the Concentration-time Curve of Melatonin From 0 to 24 Hours

Description

Area under the concentration-time curve is a measure of total drug exposure.

Time Frame

Day 15

Title

Average Cmax (Maximum Observed Plasma Concentration) Calculated as the Average of Three Highest Cmax Observations Within the Sampling Period.

Description

Average Cmax calculated as the average of three highest Cmax observations within the sampling period.

Time Frame

Day 15

10. Eligibility

Sex

All

Minimum Age & Unit of Time

18 Years

Accepts Healthy Volunteers

Eligibility Criteria

Inclusion Criteria: Females of childbearing potential who is sexually active must agree to use adequate contraception from screening throughout the duration of the study. Must have a diagnosis of Delayed Sleep Phase Syndrome according to International Classification of Sleep Disorders criteria for at least 3 months. Based on sleep history, subject's habitual sleep time is more than 3 hours later than the desired sleep time. Must have had self reported insomnia which is defined per the sleep history as his or her sleep latency of at least 45 minutes when attempting to sleep at desired sleep time required by his or her work or school schedule. The subjective sleep latency via Post sleep questionnaire during outpatient screening period must be greater than or equal to 45 minutes during every working night or school night provided the subject went to bed at their desired sleep time. During single blind placebo run-in Polysomnography screening nights, subject is instructed to go to bed at their desired bed time and must demonstrate difficulty in falling asleep based on the following criteria: During Polysomnography screening nights when the subject goes to bed at their desired sleep time or The average of total wake time Is in good health as determined by a medical and psychiatric history, physical examination, Electrocardiogram, and serum chemistry and hematology. Is able to complete self-rating scales via interactive voice response system, and has a touch tone phone. Is willing to comply with study procedures and restrictions with fixed sleep time and wake time during the study and to attend regularly scheduled clinic visits as specified in this protocol. Has a body mass index is between 18 and 34 kg/m2, inclusive. Has a negative urine test result for selected substances of abuse (including alcohol). Has a negative test result for hepatitis B surface antigen and hepatitis C virus antibody or history of human immunodeficiency virus. Has not used pharmacological sleep assistance for more than 4 times/week during the 3 months prior to Initial Screening. Must have discontinued use of all pharmacological sleep aids beginning 1 week prior to Visit 2 and for the duration of the trial. Exclusion Criteria: Has a known hypersensitivity to ramelteon or related compounds, including melatonin and melatonin-related compounds or 5-hydroxytryptophan. Has participated in any other investigational study and/or taken any investigational drug within 30 days or 5 half-lives prior to the first dose of study medication, whichever is longer. Has flown across greater than 3 time zones within the past 3 months prior to administration of study medication. Has sleep schedule changes required by employment (eg, shift worker) within 3 months prior to the administration of study medication. Has participated in a weight loss program or has substantially altered their exercise routine within 30 days prior to the administration of study medication. Has a history of alcohol abuse within the past 12 months, as defined in the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision, or regularly consumes more than 14 alcoholic drinks per week or consumes any alcoholic drinks within 24 hours of Screening Visit. Has a history of drug abuse within the past 12 months. Has a current, clinically significant neurological (including cognitive), hepatic, renal, endocrine, cardiovascular, gastrointestinal, pulmonary, hematological, or metabolic disease, as determined by the investigator. Has a probable current diagnosis of another circadian rhythm disorder or a sleep disorder other than Delayed Sleep Phase Syndrome that is the primary cause of insomnia. Had an apnea hypopnea index greater than 10 on the first night of Polysomnography Screening. Has periodic limb movements during sleep with arousal index greater than 10 as seen on the first night of Polysomnography screening only. Has a positive urine drug screen or breathalyzer test. Has ever had a history of seizures; sleep apnea, restless leg syndrome, chronic obstructive pulmonary disease, fibromyalgia, or a positive test result for the aforementioned ailments on the screening Polysomnography, schizophrenia, bipolar disorder, mental retardation, or cognitive disorder. Has a history of psychiatric disorder (including anxiety or depression) within the past 12 months. Smokes more than 3 cigarettes per day or uses tobacco products during nightly awakenings. Routinely consumes caffeine including coffee, tea and/or other caffeine-containing beverages or food averaging more than 600 mg of caffeine per day. Has used any central nervous system drug or other medications, including those used to treat psychiatric disorders, known to affect sleep/wake function within 1 week whichever is longer prior to the administration of single blind study drug. Used melatonin, or other drugs/supplements known to affect sleep/wake function within 1 week (or 5 half lives of the drug) whichever is longer prior to the first dose of single blind medication. Is required to take or intends to continue taking any disallowed medication, any prescription medication, herbal treatment or over-the counter medication that may interfere with evaluation of the study medication, including: Anxiolytics Hypnotics Antidepressants Anticonvulsants Sedating H1 antihistamines Systemic steroids Respiratory stimulants Decongestants Antipsychotics Muscle relaxants Over-the-counter and prescription diet aids Narcotic analgesics Beta Blockers St. John's wort Kava kava Ginkgo biloba Modafinil Coumadin Heparin Melatonin and all other drugs or supplements known to affect sleep/wake function will be prohibited within 1 week of the first dose of study medication and during the entire study. Has any clinically important abnormal finding as determined by a medical history, physical examination, Electrocardiogram, or clinical laboratory tests as determined by the investigator. Has a positive hepatitis panel including anti- Hepatitis A Virus, hepatitis B surface antigen or anti- hepatitis C virus. Has any additional condition(s) that in the investigator's opinion would: Affect sleep/wake function Prohibit the subject from completing the study, or Not be in the best interest of the subject. Exhibits a placebo response during single-blinded placebo run in period. Individuals with a habitual sleep time later than 4:00 am should not be included in the study.

Overall Study Officials:

First Name & Middle Initial & Last Name & Degree

Medical Director Clinical Science

Organizational Affiliation

Takeda

Official's Role

Study Director

Facility Information:

City

Birmingham

State/Province

Alabama

Country

United States

City

Tucson

State/Province

Arizona

Country

United States

City

Hot Springs

State/Province

Arkansas

Country

United States

City

Little Rock

State/Province

Arkansas

Country

United States

City

Fountain Valley

State/Province

California

Country

United States

City

Glendale

State/Province

California

Country

United States

City

Los Angeles

State/Province

California

Country

United States

City

San Diego

State/Province

California

Country

United States

City

Santa Monica

State/Province

California

Country

United States

City

Tustin

State/Province

California

Country

United States

City

Colorado Springs

State/Province

Colorado

Country

United States

City

Hallandale Bch

State/Province

Florida

Country

United States

City

Naples

State/Province

Florida

Country

United States

City

Pembroke Pines

State/Province

Florida

Country

United States

City

South Miami

State/Province

Florida

Country

United States

City

Spring Hill

State/Province

Florida

Country

United States

City

St. Petersburg

State/Province

Florida

Country

United States

City

Winter Park

State/Province

Florida

Country

United States

City

Atlanta

State/Province

Georgia

Country

United States

City

Gainesville

State/Province

Georgia

Country

United States

City

Macon

State/Province

Georgia

Country

United States

City

Chicago

State/Province

Illinois

Country

United States

City

Danville

State/Province

Indiana

Country

United States

City

Overland Park

State/Province

Kansas

Country

United States

City

Topeka

State/Province

Kansas

Country

United States

City

Crestview Hills

State/Province

Kentucky

Country

United States

City

Paducah

State/Province

Kentucky

Country

United States

City

Chevy Chase

State/Province

Maryland

Country

United States

City

Newton

State/Province

Massachusetts

Country

United States

City

Hattiesburg

State/Province

Mississippi

Country

United States

City

Lincoln

State/Province

Nebraska

Country

United States

City

Las Vegas

State/Province

Nevada

Country

United States

City

New York

State/Province

New York

Country

United States

City

Raleigh

State/Province

North Carolina

Country

United States

City

Salisbury

State/Province

North Carolina

Country

United States

City

Cincinnati

State/Province

Ohio

Country

United States

City

Dublin

State/Province

Ohio

Country

United States

City

Toledo

State/Province

Ohio

Country

United States

City

Salem

State/Province

Oregon

Country

United States

City

Clarks Summit

State/Province

Pennsylvania

Country

United States

City

Columbia

State/Province

South Carolina

Country

United States

City

Austin

State/Province

Texas

Country

United States

12. IPD Sharing Statement

Learn more about this trial

Efficacy of Ramelteon on Speeding Up Sleep in Subjects With Delayed Sleep Phase Syndrome

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