Clinical trial

Comparison of the Efficacy and Tolerability of Black Cohosh Vs Tibolone in…

NCT00299364 · Schaper & Bruemmer GmbH & Co KG, Industry · Completed

Key facts

NCT number NCT00299364
Title Comparison of the Efficacy and Tolerability of Black Cohosh Vs Tibolone in Patients With Menopausal Symptoms
Official title Multi-Center, Randomized, Double-Blind, Parallel-Controlled Study on the Efficacy and Tolerability of Black Cohosh Vs Tibolone in Patients With Menopausal Symptoms
Lead sponsor Schaper & Bruemmer GmbH & Co KG, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Menopause
Intervention type Drug
Interventions Black Cohosh (iCR) or tibolone
Enrollment 240
Start date Sep 1, 2004
Completion May 1, 2005
First posted Mar 6, 2006
Last update posted Mar 6, 2006
Countries China

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies