drugset / Trial / NCT00152438

Vasomotor Symptoms (VMS) Progesterone Study: Vasomotor Symptoms and Endothelial Function - Trial of Oral Micronized Progesterone

NCT00152438

Phase 2 Unknown 125 enrolled University of British Columbia
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary purpose of this study is to determine the effects of a full dose (300 mg at hs) of oral micronized progesterone (OMP) on vasomotor symptoms \[VMS\] (hot flushes/night sweats), on forearm blood flow and on lipid levels and blood pressure in menopausal women without cardiovascular disease and with moderate to severe VMS. The hypotheses are that progesterone will improve hot flushes, increase endothelium-dependent forearm blood flow and will decrease blood pressure without change in lipid levels.

Timeline

Start
2005-09
Primary completion
2009-10
Completion
2012-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Progesterone Other / unclassified 300 mg Oral

Indications

No indication recorded.