drugset / Trial / NCT03034018

Efficacy of Suvorexant in the Treatment of Hot Flash-associated Insomnia

NCT03034018 ↗

Phase 4 Completed 60 enrolled Brigham and Women's Hospital
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The aim of this study is to determine the effect of suvorexant on insomnia symptoms in peri- and postmenopausal women who are experiencing sleep difficulties related to nighttime hot flashes.

Timeline

Start
2017-05-25
Primary completion
2020-04-03
Completion
2020-04-03

Outcome

Met primary endpoint

paper was greater on suvorexant (-8.1 [95% CI, -10.2 to -6.0]) compared to placebo (-5.6 [95% CI, -7.4 to -3.9], p = .04). PMID 35022783 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Suvorexant Small molecule 10 mg Oral
Subject Suvorexant Small molecule 20 mg Oral

Indications