Clinical Trials Directory

Trials / Completed

CompletedNCT00332553

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

Study of Vasomotor Symptoms in Postmenopausal Women Receiving Combination Raloxifene and Oral Estrogen

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
150 (planned)
Sponsor
Eli Lilly and Company · Industry
Sex
Female
Age
50 Years – 70 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGRaloxifene
DRUGmedroxyprogesterone acetate
DRUGestrogen
DRUG17 beta estradiol

Timeline

Start date
2002-02-01
Completion
2004-05-01
First posted
2006-06-01
Last updated
2007-05-15

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00332553. Inclusion in this directory is not an endorsement.