drugset / Trial / NCT00332553

Study of Hot Flashes and Night Sweats in Postmenopausal Women Receiving Combination Raloxifene and Oral Estrogen

NCT00332553

Phase 2 Completed 150 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindPrevention

Summary

This pilot study was designed to explore the effects of combined treatment with raloxifene HCl 60 mg and oral 17 beta-estradiol 1mg/day on the number of vasomotor episodes (hot flashes plus night sweats) in postmenopausal women discontinuing continuous combined hormone replacement therapy (ccHRT) compared to women treated with raloxifene HCl 60 mg alone.

Timeline

Start
2002-02
Primary completion
Completion
2004-05

Drugs

EvaluationDrugModalityDoseRoute
Subject 17-beta estradiol Unknown 1 mg Oral
Subject Raloxifene Other / unclassified 60 mg
Background medroxyprogesterone acetate Other / unclassified

Indications

No indication recorded.