- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02452684
Investigation of the Safety and Efficacy of Eszopiclone in Insomnia Patients
September 6, 2018 updated by: Eisai Co., Ltd.
Investigation of the Safety and Efficacy of Eszopiclone in Insomnia Patients (Study LUN01S)
To investigate the safety and efficacy of administration of eszopiclone for 4 weeks in insomnia patients.
Study Overview
Study Type
Observational
Enrollment (Actual)
4876
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Osaka, Japan
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Tokyo, Japan
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Insomnia participants who did not take eszopiclone before assessment
Description
Inclusion Criteria:
- Insomnia participants who did not take eszopiclone before assessment
- Participants who receive assessment by using sleep questionaries
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
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Participants with insomnia
Participants with insomnia who will receive eszopiclone, per approved label.
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The usual dosage of eszopiclone is 2 mg per dose for adults and 1 mg per dose for elderly participants, taken orally before bedtime.
The dosage may be adjusted according to the participant's symptoms, but a single dose should not exceed 3 mg in adults and 2 mg in elderly participants.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Assessment of overall improvement
Time Frame: Up to 4 weeks
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Participants will be interviewed regarding sleep improvement at 4 weeks after first dose or discontinuation relative to predose, and select the appropriate answer of: 1. Improved 2. Unchanged 3. Worse 4. Indiscernible
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Up to 4 weeks
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Number of participants with adverse events (AEs)
Time Frame: Up to 4 weeks
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Up to 4 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Akira Endo, Drug Fostering and Evolution Coordination Department, Corporate Medical Affairs Headquarters, Eisai Co., Ltd.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Japanese Journal of Sleep Medicine 10 : 425-441, 2016.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 1, 2012
Primary Completion (Actual)
November 11, 2014
Study Completion (Actual)
December 22, 2015
Study Registration Dates
First Submitted
May 19, 2015
First Submitted That Met QC Criteria
May 20, 2015
First Posted (Estimate)
May 25, 2015
Study Record Updates
Last Update Posted (Actual)
September 7, 2018
Last Update Submitted That Met QC Criteria
September 6, 2018
Last Verified
January 1, 2017
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- LUN01S
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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