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Long Term Treatment With Zolpidem: Nightly and Intermittent Dosing

Primary Purpose

Insomnia, Primary Insomnia, Psychophysiologic Insomnia

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Zolpidem
Sugar Pill
Sponsored by
University of Rochester
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Insomnia focused on measuring Insomnia, Sleep, zolpidem, Ambien, Hypnotics

Eligibility Criteria

25 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Ages 25 - 55 a stable sleep/wake schedule with a preferred sleep phase between 10:00 p.m. and 8:00 a.m. Patients with Primary Insomnia will meet diagnostic criteria for Psychophysiologic Insomnia according to the International Classification of Sleep Disorders manual (ICSD). complaint of disturbed sleep must have the following characteristics: >30 minutes to fall asleep, and/or >30 minutes wake after sleep onset time, a total sleep time of no more than 6.5 hours (or a sleep efficiency of less than 85%), a problem frequency of >4 nights/ week and a problem duration >6 months. Exclusion Criteria: Unstable medical or psychiatric illness Use of medication that may cause insomnia or may be reduce the effectiveness of zolpidem (e.g. selective serotonin reuptake inhibitors(SSRI's), steroids, bronchodilators, calcium channel blockers, beta blockers, etc.) symptoms suggestive of sleep disorders other than insomnia polysomnographic data indicating sleep disorders other than insomnia Evidence of active illicit substance use or fitting criteria for alcohol abuse or dependence inadequate language comprehension pregnancy first-degree relatives with bipolar disorder or schizophrenia

Sites / Locations

  • University of Rochester Sleep Research Laboratory

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Placebo Comparator

Active Comparator

Experimental

No Intervention

Arm Label

Placebo

QHS Zolpidem

Intermittant Zolpidem

Control

Arm Description

QHS dosing with placebo (i.e. nightly dose)

QHS dosing with 10mg of zolpidem (i.e. nightly dose)

Intermittent dosing with 10mg of zolpidem (3-5 pills per week as needed

Monitor only condition (no placebo, no drug).

Outcomes

Primary Outcome Measures

Sleep Latency (SL)
Number of subjects with any reduction in SL (time to fall asleep in minutes)at post-tx compared to baseline where mean SL = mean of daily values for one week calculated from sleep diary values.

Secondary Outcome Measures

Wake After Sleep Onset (WASO)
Number of subjects with any reduction in WASO at post-tx compared to baseline where mean WASO = mean of daily values for one week calculated from sleep diary values.

Full Information

First Posted
September 7, 2005
Last Updated
October 21, 2015
Sponsor
University of Rochester
Collaborators
Sanofi-Synthelabo
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1. Study Identification

Unique Protocol Identification Number
NCT00156533
Brief Title
Long Term Treatment With Zolpidem: Nightly and Intermittent Dosing
Official Title
Long Term Treatment With Zolpidem: The Relative Efficacy of Nightly (Quaque Hora Somni [QHS]) & Intermittent Dosing and the Potential for Long Term Clinical Gains After Treatment Discontinuation.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2015
Overall Recruitment Status
Completed
Study Start Date
March 2005 (undefined)
Primary Completion Date
February 2008 (Actual)
Study Completion Date
February 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Rochester
Collaborators
Sanofi-Synthelabo

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
We want to assess whether "how and when" one takes sleep medication results in similar or different outcomes with respect to symptom relief. We also want to know whether taking medication for a period of time provides continued benefit once the medication is stopped.
Detailed Description
To date, the aggressive treatment (Tx) of chronic insomnia has been evaluated in terms of whether maintenance therapy is possible. While what constitutes maintenance therapy is a matter of debate, there are two studies which show that benzodiazepine receptor agonists (BZRAs) 1) are effective when used intermittently for up to 3 months and 2) may be used on a nightly basis for up to 6 months with no loss of efficacy. The significance of the present research is two fold. First, it will allow us to compare the two primary strategies used for long term treat of insomnia (nightly dosing vs intermittent dosing). Second, it will allow an evaluation of the possibility that extended treatment, given careful withdrawal from medication, may yield long term clinical gains. Re: Objective 1: It is widely assumed that intermittent dosing confers increased efficacy. That is, less frequent medication use will extend the duration of time for which the medication is maximally potent. An empirical assessment of this proposition is required. If incorrect, physicians and patients should be encouraged to adopt a more aggressive approach to treatment. If correct, physicians and patients should be encouraged to adopt the intermittent dosing approach to treatment. Re: Objective 2: It is widely assumed that treatment with sedatives (sleep promoting medications) constitutes only palliative care. An empirical assessment of this proposition is required. If correct, physicians and patients should be encouraged to adopt a more aggressive approach to long term treatment. If incorrect, physicians and patients should be encouraged to adopt an approach to treatment that is not currently a standard of practice: extended treatment with a clear plan to taper medication that is designed to maintain the clinical gains that occurred with medication use. We propose to evaluate the above issues in a pilot study of 40 subjects with Primary Insomnia where subjects are randomized to one of 4 conditions: QHS dosing with placebo QHS dosing with 10mg of zolpidem Intermittent dosing with 10mg of zolpidem (3-5 pills per week as needed) Monitor only condition.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insomnia, Primary Insomnia, Psychophysiologic Insomnia
Keywords
Insomnia, Sleep, zolpidem, Ambien, Hypnotics

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
QHS dosing with placebo (i.e. nightly dose)
Arm Title
QHS Zolpidem
Arm Type
Active Comparator
Arm Description
QHS dosing with 10mg of zolpidem (i.e. nightly dose)
Arm Title
Intermittant Zolpidem
Arm Type
Experimental
Arm Description
Intermittent dosing with 10mg of zolpidem (3-5 pills per week as needed
Arm Title
Control
Arm Type
No Intervention
Arm Description
Monitor only condition (no placebo, no drug).
Intervention Type
Drug
Intervention Name(s)
Zolpidem
Other Intervention Name(s)
Ambien
Intervention Description
10 mg of Zolpidem
Intervention Type
Drug
Intervention Name(s)
Sugar Pill
Primary Outcome Measure Information:
Title
Sleep Latency (SL)
Description
Number of subjects with any reduction in SL (time to fall asleep in minutes)at post-tx compared to baseline where mean SL = mean of daily values for one week calculated from sleep diary values.
Time Frame
Baseline and Post-treatment (12wks)
Secondary Outcome Measure Information:
Title
Wake After Sleep Onset (WASO)
Description
Number of subjects with any reduction in WASO at post-tx compared to baseline where mean WASO = mean of daily values for one week calculated from sleep diary values.
Time Frame
Baseline and Post-Treatment (12 weeks)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ages 25 - 55 a stable sleep/wake schedule with a preferred sleep phase between 10:00 p.m. and 8:00 a.m. Patients with Primary Insomnia will meet diagnostic criteria for Psychophysiologic Insomnia according to the International Classification of Sleep Disorders manual (ICSD). complaint of disturbed sleep must have the following characteristics: >30 minutes to fall asleep, and/or >30 minutes wake after sleep onset time, a total sleep time of no more than 6.5 hours (or a sleep efficiency of less than 85%), a problem frequency of >4 nights/ week and a problem duration >6 months. Exclusion Criteria: Unstable medical or psychiatric illness Use of medication that may cause insomnia or may be reduce the effectiveness of zolpidem (e.g. selective serotonin reuptake inhibitors(SSRI's), steroids, bronchodilators, calcium channel blockers, beta blockers, etc.) symptoms suggestive of sleep disorders other than insomnia polysomnographic data indicating sleep disorders other than insomnia Evidence of active illicit substance use or fitting criteria for alcohol abuse or dependence inadequate language comprehension pregnancy first-degree relatives with bipolar disorder or schizophrenia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael L Perlis, Ph.D.
Organizational Affiliation
University of Rochester
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Rochester Sleep Research Laboratory
City
Rochester
State/Province
New York
ZIP/Postal Code
14642
Country
United States

12. IPD Sharing Statement

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Long Term Treatment With Zolpidem: Nightly and Intermittent Dosing

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