drugset / Trial / NCT00672061

Safety of Ramelteon in Subjects With Mild to Moderate Obstructive Sleep Apnea

NCT00672061 ↗

Phase 2 Completed 26 enrolled Takeda
RandomizedCrossoverQuadruple-blindTreatment

Summary

The purpose of this study is to assess the safety of ramelteon, once daily (QD), in individuals with obstructive sleep apnea.

Timeline

Start
2003-07
Primary completion
2003-12
Completion
2003-12

Outcome

Missed primary endpoint

paper Apnea-hypopnea index was similar in ramelteon and placebo groups (11.4 vs 11.1, respectively; CI = -2.1, 2.6, P = 0.812). PMID 17294232 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Ramelteon Unknown 16 mg Oral