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Last Updated: December 15, 2024

CLINICAL TRIALS PROFILE FOR ESZOPICLONE


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All Clinical Trials for Eszopiclone

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00120250 ↗ Eszopiclone for Sleep Disturbance and Nightmares in Post-Traumatic Stress Disorder Completed Massachusetts General Hospital Phase 4 2005-06-01 The purpose of this study is to obtain data investigating the safety and efficacy of eszopiclone for the treatment of post-traumatic stress disorder (PTSD)-related sleep disturbance and the impact of improved sleep with eszopiclone treatment on neuroendocrine correlates of PTSD. The investigators hypothesize that eszopiclone will be significantly more effective than placebo and well tolerated for PTSD-related sleep disturbance, improvement in sleep will be associated with improvement in overall PTSD symptoms, and patients with PTSD-related sleep disturbances will have abnormal levels of stress hormones.
NCT00167375 ↗ Testing the Nocturnal Sleep Latency Profile in Primary Insomnia Completed American Academy of Sleep Medicine 2005-01-01 This study tests a new kind of sleep study in which subjects are awakened 2 times after initially going to sleep. The study focuses on the EEG signal process as a person goes to sleep. The general hypothesis is that the signal properties are stable from night to night during baseline studies, and are different between controls and patients with primary insomnia. The primary insomnia patients then go on to have about 2 weeks of an insomnia intervention. Then the new kind of study is repeated in the patients. The controls only are examined in baseline studies.
NCT00167375 ↗ Testing the Nocturnal Sleep Latency Profile in Primary Insomnia Completed Sunovion 2005-01-01 This study tests a new kind of sleep study in which subjects are awakened 2 times after initially going to sleep. The study focuses on the EEG signal process as a person goes to sleep. The general hypothesis is that the signal properties are stable from night to night during baseline studies, and are different between controls and patients with primary insomnia. The primary insomnia patients then go on to have about 2 weeks of an insomnia intervention. Then the new kind of study is repeated in the patients. The controls only are examined in baseline studies.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Eszopiclone

Condition Name

Condition Name for Eszopiclone
Intervention Trials
Insomnia 27
Obstructive Sleep Apnea 11
Primary Insomnia 10
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Condition MeSH

Condition MeSH for Eszopiclone
Intervention Trials
Sleep Initiation and Maintenance Disorders 43
Sleep Apnea, Obstructive 13
Sleep Apnea Syndromes 11
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Clinical Trial Locations for Eszopiclone

Trials by Country

Trials by Country for Eszopiclone
Location Trials
United States 303
Japan 24
United Kingdom 6
India 3
Ukraine 2
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Trials by US State

Trials by US State for Eszopiclone
Location Trials
Massachusetts 21
California 18
Pennsylvania 13
Ohio 12
New Jersey 11
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Clinical Trial Progress for Eszopiclone

Clinical Trial Phase

Clinical Trial Phase for Eszopiclone
Clinical Trial Phase Trials
Phase 4 25
Phase 3 16
Phase 2/Phase 3 2
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Clinical Trial Status

Clinical Trial Status for Eszopiclone
Clinical Trial Phase Trials
Completed 56
Recruiting 6
Terminated 3
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Clinical Trial Sponsors for Eszopiclone

Sponsor Name

Sponsor Name for Eszopiclone
Sponsor Trials
Sunovion 35
University of California, San Diego 5
Massachusetts General Hospital 5
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Sponsor Type

Sponsor Type for Eszopiclone
Sponsor Trials
Other 53
Industry 49
NIH 8
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