Investigation of the Safety and Efficacy of Eszopiclone in Insomnia Patients
NCT ID: NCT02452684
Last Updated: 2018-09-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
4876 participants
OBSERVATIONAL
2012-10-01
2015-12-22
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Participants with insomnia
Participants with insomnia who will receive eszopiclone, per approved label.
Eszopiclone
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.
Interventions
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Eszopiclone
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 Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Participants who receive assessment by using sleep questionaries
ALL
No
Sponsors
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Eisai Co., Ltd.
INDUSTRY
Responsible Party
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Principal Investigators
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Akira Endo
Role: STUDY_DIRECTOR
Drug Fostering and Evolution Coordination Department, Corporate Medical Affairs Headquarters, Eisai Co., Ltd.
Locations
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Osaka, , Japan
Tokyo, , Japan
Countries
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References
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Japanese Journal of Sleep Medicine 10 : 425-441, 2016.
Other Identifiers
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LUN01S
Identifier Type: -
Identifier Source: org_study_id
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