Clinical Trials Directory

Trials / Completed

CompletedNCT00005623

Cyproterone Acetate in Treating Hot Flashes Following Surgical or Chemical Castration for Prostate Cancer

A Phase III, Randomized, Multicenter, Placebo-Controlled, Double-Blind Clinical Trial to Study the Efficacy and Safety of CyPat (Cyproterone Acetate [CA]) for the Treatment of Hot Flashes Following Surgical or Chemical Castration of Prostate Cancer Patients and Its Impact on the Quality of Life in These Patients

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
Sponsor
Barr Laboratories · Industry
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Cyproterone acetate may be effective treatment for hot flashes following surgical or chemical castration for prostate cancer. It is not yet known which regimen of cyproterone acetate is more effective for hot flashes. PURPOSE: Randomized phase III trial to determine the effectiveness of cyproterone acetate in treating patients who have hot flashes following surgical or chemical castration for prostate cancer.

Detailed description

OBJECTIVES: * Determine the efficacy of cyproterone acetate in patients with hot flashes following bilateral orchiectomy or medical castration for prostate cancer. * Compare the effectiveness of two doses of cyproterone acetate in these patients. * Determine the safety of this regimen in these patients. * Determine the impact of this regimen on the quality of life of these patients. OUTLINE: This is a randomized, double-blind, placebo controlled study. Patients receive one of two doses of oral cyproterone acetate or placebo for 12 weeks, followed by a 6-9 month open label extension period with all patients receiving cyproterone acetate. Quality of life is assessed. PROJECTED ACCRUAL: Not specified

Conditions

Interventions

TypeNameDescription
DRUGcyproterone acetate
PROCEDUREquality-of-life assessment

Timeline

Start date
1999-12-01
Completion
2004-01-01
First posted
2003-01-27
Last updated
2013-03-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00005623. Inclusion in this directory is not an endorsement.