Clinical Trials Directory

Trials / Completed

CompletedNCT00195520

Study Evaluating Totelle® in Menopausal Symptoms and Sexual Function

An Open Assessment of the Effect of Low-Dose Totelle® 1 mg on Menopausal Symptoms, Sexual Function and Quality of Life

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer · Industry
Sex
Female
Age
45 Years – 60 Years
Healthy volunteers
Not accepted

Summary

To evaluate the tolerability, bleeding patterns and acceptability of Totelle® 1mg administered to a population of Brazilian women in a continuous combined regime for hormone replacement therapy.

Conditions

Interventions

TypeNameDescription
DRUGTotelle®

Timeline

Start date
2004-12-01
Completion
2006-12-01
First posted
2005-09-19
Last updated
2008-08-05

Locations

2 sites across 1 country: Brazil

Source: ClinicalTrials.gov record NCT00195520. Inclusion in this directory is not an endorsement.