drugset / Trial / NCT00316992

Safety of Ramelteon in Subjects With Chronic Obstructive Pulmonary Disease

NCT00316992 ↗

Phase 4 Completed 25 enrolled Takeda
RandomizedCrossoverQuadruple-blindTreatment

Summary

The purpose of this study is to determine if ramelteon has respiratory depressant effects in subjects with moderate to severe chronic obstructive pulmonary disease.

Timeline

Start
2006-04
Primary completion
2006-11
Completion
2006-11

Outcome

Missed primary endpoint

paper No significant difference in SaO(2) for the entire night was observed with ramelteon vs placebo (92.2% vs 92.5%, P = 0.576). PMID 18584227 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Ramelteon Unknown 8 mg Oral