Trials / Completed
CompletedNCT00367965
Study of Eszopiclone Compared to Placebo on Daytime Function in Subjects With Insomnia Related to Rheumatoid Arthritis
The Effect of Eszopiclone 3 mg Compared to Placebo on Daytime Function in Subjects With Insomnia Related to Rheumatoid Arthritis
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 153 (actual)
- Sponsor
- Sumitomo Pharma America, Inc. · Industry
- Sex
- All
- Age
- 25 Years – 64 Years
- Healthy volunteers
- Not accepted
Summary
To demonstrate subjective sleep efficacy of eszopiclone 3 mg in subjects with insomnia related to rheumatoid arthritis (RA).
Detailed description
A multicenter, randomized, double-blind, placebo controlled, parallel group study of eszopiclone 3 mg in subjects with insomnia related to rheumatoid arthritis. This study was previously posted by Sepracor Inc. In October 2009, Sepracor Inc. was acquired by Dainippon Sumitomo Pharma., and in October 2010, Sepracor Inc's name was changed to Sunovion Pharmaceuticals Inc.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Eszopiclone | eszopiclone 3 mg |
| DRUG | placebo | placebo tablet |
Timeline
- Start date
- 2004-02-01
- Primary completion
- 2004-11-01
- Completion
- 2004-11-01
- First posted
- 2006-08-24
- Last updated
- 2012-02-22
Locations
38 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00367965. Inclusion in this directory is not an endorsement.