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Treatment of Insomnia in Migraineurs

Primary Purpose

Insomnia, Migraine

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
eszopiclone
placebo
Sponsored by
MedVadis Research Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Insomnia focused on measuring insomnia, migraine, eszopiclone, insomnia in migraineurs

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers
Subjects included in the study are men and women, 18 to 64 years of age (inclusive), with IHS-II migraine with/without aura and DSM-IV primary insomnia (sleep onset/sleep maintenance). The required migraine frequency is 4-12 times per month, with a maximum of 20 days with headache per month, for 1 month or longer prior to screening. The requirement with regard to insomnia is a usual, estimated total sleep time of 6½ hours per night or less, for 1 month or longer prior to screening, due to problems falling asleep, waking up during the night, or waking up early. The sleep and headache eligibility criteria are confirmed at the randomization visit on the basis of the daily diary.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Eszopiclone (Lunesta) 3mg

    Placebo

    Arm Description

    Participants with IHS-II migraine with and/or without aura and with DSM-IV primary insomnia. They were treated for 6 weeks with 3mg eszopiclone, followed by a 2-week runout period. Participants came in for five visits: a screening visit, a randomization visit, a compliance visit, an end-treatment visit, and an exit/early termination visit.

    Participants with IHS-II migraine with and/or without aura and with DSM-IV primary insomnia. They were treated for 6 weeks with placebo, followed by a 2-week runout period. Participants came in for five visits: a screening visit, a randomization visit, a compliance visit, an end-treatment visit, and an exit/early termination visit.

    Outcomes

    Primary Outcome Measures

    Total Sleep Time
    Participants were asked to record an estimated total time asleep on a daily basis. Nightly estimates were averaged over a 2 week period for baseline and 6 week period so that the total sleep time represents the average total time asleep each night.

    Secondary Outcome Measures

    Nighttime Awakenings
    Participants were asked to keep a daily record. 6 week data were averaged over the 6 week period
    Nighttime Awakenings
    Participants were asked to keep a daily record. The average among weeks 1 and 2, weeks 3 and 4, and weeks 5 and 6 were taken, resulting in 3 averages, where the lowest average is reported as the minimum value of the full range, the middle average is reported as the median, and the highest average is reported as the maximum value of the full range
    Quality of Sleep
    Participants were asked to keep a daily record. 6 week data were averaged over the 6 week period Overall sleep quality was measured on a scale of 1=poor to 10=excellent. Daytime alertness was measured on a scale of 1=not alert to 10=extremely alert. Daytime fatigue was measured on a scale of 1=not tired to 10=extremely tired. Daytime functioning was measured on a scale of 1=poor to 10=excellent.
    Daytime Fatigue
    Participants were asked to keep a daily record. Daytime fatigue was measured on a scale of 1=not tired to 10=extremely tired. The average among weeks 1 and 2, weeks 3 and 4, and weeks 5 and 6 were taken, resulting in 3 averages, where the lowest average is reported as the minimum value of the full range, the middle average is reported as the median, and the highest average is reported as the maximum value of the full range
    Headache Frequency
    Number of days per week in which a participant had a headache. Participants were asked to keep a daily record. 6 week data were averaged over the 6 week period
    Headache Duration
    Participants were asked to keep a daily record. 6 week data were averaged over the 6 week period
    Headache Intensity
    Participants were asked to keep a daily record. 6 week data were averaged over the 6 week period Headache intensity was measured on a scale of 1=not intense to 10=worst headache possible

    Full Information

    First Posted
    December 18, 2008
    Last Updated
    May 19, 2023
    Sponsor
    MedVadis Research Corporation
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00812214
    Brief Title
    Treatment of Insomnia in Migraineurs
    Official Title
    Treatment of Insomnia in Migraineurs With Eszopiclone (Lunesta™) and Its Effect on Sleep Time, Headache Frequency, and Daytime Functioning: a Randomized, Double-blind, Placebo-controlled, Parallel-group Pilot Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2023
    Overall Recruitment Status
    Completed
    Study Start Date
    April 2007 (undefined)
    Primary Completion Date
    September 2008 (Actual)
    Study Completion Date
    September 2008 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    MedVadis Research Corporation

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    It is hypothesized that treating insomnia in migraineurs, many of whom also have tension headaches, prolongs total sleep time to the extent that it decreases overall headache frequency. Chronic headache sufferers also feel more tired during the day, undoubtedly affecting daytime functioning, which is hypothesized to improve as well with prolonged total sleep time.
    Detailed Description
    The objective of the study is to determine the effect of prolonging total sleep time in migraineurs with insomnia on overall headache frequency, daytime alertness, fatigue, and functioning. The prolongation of total sleep time is accomplished by bedtime administration of 3 mg eszopiclone (Lunesta™), compared with placebo through a parallel-group design.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Insomnia, Migraine
    Keywords
    insomnia, migraine, eszopiclone, insomnia in migraineurs

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    113 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Eszopiclone (Lunesta) 3mg
    Arm Type
    Experimental
    Arm Description
    Participants with IHS-II migraine with and/or without aura and with DSM-IV primary insomnia. They were treated for 6 weeks with 3mg eszopiclone, followed by a 2-week runout period. Participants came in for five visits: a screening visit, a randomization visit, a compliance visit, an end-treatment visit, and an exit/early termination visit.
    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    Participants with IHS-II migraine with and/or without aura and with DSM-IV primary insomnia. They were treated for 6 weeks with placebo, followed by a 2-week runout period. Participants came in for five visits: a screening visit, a randomization visit, a compliance visit, an end-treatment visit, and an exit/early termination visit.
    Intervention Type
    Drug
    Intervention Name(s)
    eszopiclone
    Other Intervention Name(s)
    Lunesta
    Intervention Description
    3 mg tablet every night at bedtime
    Intervention Type
    Drug
    Intervention Name(s)
    placebo
    Intervention Description
    1 tablet every night at bedtime
    Primary Outcome Measure Information:
    Title
    Total Sleep Time
    Description
    Participants were asked to record an estimated total time asleep on a daily basis. Nightly estimates were averaged over a 2 week period for baseline and 6 week period so that the total sleep time represents the average total time asleep each night.
    Time Frame
    Baseline, 6 weeks
    Secondary Outcome Measure Information:
    Title
    Nighttime Awakenings
    Description
    Participants were asked to keep a daily record. 6 week data were averaged over the 6 week period
    Time Frame
    Baseline, 6 weeks
    Title
    Nighttime Awakenings
    Description
    Participants were asked to keep a daily record. The average among weeks 1 and 2, weeks 3 and 4, and weeks 5 and 6 were taken, resulting in 3 averages, where the lowest average is reported as the minimum value of the full range, the middle average is reported as the median, and the highest average is reported as the maximum value of the full range
    Time Frame
    Measured every two weeks (1&2, 3&4, 5&6)
    Title
    Quality of Sleep
    Description
    Participants were asked to keep a daily record. 6 week data were averaged over the 6 week period Overall sleep quality was measured on a scale of 1=poor to 10=excellent. Daytime alertness was measured on a scale of 1=not alert to 10=extremely alert. Daytime fatigue was measured on a scale of 1=not tired to 10=extremely tired. Daytime functioning was measured on a scale of 1=poor to 10=excellent.
    Time Frame
    Baseline, 6 weeks
    Title
    Daytime Fatigue
    Description
    Participants were asked to keep a daily record. Daytime fatigue was measured on a scale of 1=not tired to 10=extremely tired. The average among weeks 1 and 2, weeks 3 and 4, and weeks 5 and 6 were taken, resulting in 3 averages, where the lowest average is reported as the minimum value of the full range, the middle average is reported as the median, and the highest average is reported as the maximum value of the full range
    Time Frame
    Measured every two weeks (1&2, 3&4, 5&6)
    Title
    Headache Frequency
    Description
    Number of days per week in which a participant had a headache. Participants were asked to keep a daily record. 6 week data were averaged over the 6 week period
    Time Frame
    Baseline, 6 weeks
    Title
    Headache Duration
    Description
    Participants were asked to keep a daily record. 6 week data were averaged over the 6 week period
    Time Frame
    Baseline, 6 weeks
    Title
    Headache Intensity
    Description
    Participants were asked to keep a daily record. 6 week data were averaged over the 6 week period Headache intensity was measured on a scale of 1=not intense to 10=worst headache possible
    Time Frame
    Baseline, 6 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion criteria: Men and women, 18 to 64 years of age (inclusive) with International Headache Society (IHS)-II migraine with/without aura and Diagnostic and Statistical Manual (DSM)-IV primary insomnia (sleep onset/sleep maintenance). Migraine frequency is 4-12 times per month, with a maximum of 20 days with headache per month, for 1 month or longer prior to screening. A usual, estimated total sleep time of 6½ hours per night or less, for 1 month or longer prior to screening, due to problems falling asleep, waking up during the night, or waking up early. Exclusion criteria: Abortive migraine treatment with schedule II-III opioids. Use of caffeine-containing medications, prescription and non-prescription, not exceeding 10 days per month. Preventive migraine treatment with tricyclics or anticonvulsants. Treatment of insomnia with non-prescription medications, such as diphenhydramine, melatonin, or valerian, and prescription medications, such as hypnotics, barbiturates, benzodiazepines, sedating antihistamines, antidepressants, and antipsychotics.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Egilius LH Spierings, M.D., Ph.D.
    Organizational Affiliation
    MedVadis Research Corporation
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    25323219
    Citation
    Spierings EL, McAllister PJ, Bilchik TR. Efficacy of treatment of insomnia in migraineurs with eszopiclone (Lunesta(R)) and its effect on total sleep time, headache frequency, and daytime functioning: A randomized, double-blind, placebo-controlled, parallel-group, pilot study. Cranio. 2015 Apr;33(2):115-21. doi: 10.1179/0886963414Z.00000000084. Epub 2014 Oct 16.
    Results Reference
    result

    Learn more about this trial

    Treatment of Insomnia in Migraineurs

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