drugset / Trial / NCT00756002
Safety and Efficacy Study of Ramelteon in Subjects With Chronic Insomnia
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study is to determine the safety and efficacy of 4 mg of Ramelteon, once daily (QD), in subjects with chronic insomnia.
Timeline
- Start
- 2007-08
- Primary completion
- 2008-03
- Completion
- 2008-03
Outcome
Met primary endpoint
registry analysis (superiority or other test); Placebo QD vs Ramelteon 4 mg QD; p <0.001; ANCOVA NCT00756002 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ramelteon | Unknown | 4 mg | Oral |