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Tibolone Endometrium Study (Study 32972)(P06470) — THEBES  

Postmenopausal Women Clinical Trial

Official title:
A Multinational, Multicenter, Randomized, Double-blind, Parallel Group, Active Controlled, Comparative Trial, to Assess the Endometrial Histological Profile Following Treatment With Tibolone (Org OD14) Versus Conjugated Estrogen (CE) Plus Medroxyprogesterone Acetate (MPA) in Postmenopausal Women

Clinical Trial Summary

Tibolone has been registered for the treatment of climacteric symptoms and for the prevention of postmenopausal osteoporosis. This is a 2-year study to further confirm the endometrial safety of tibolone in comparison with CE/MPA.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00745108
Study type Interventional
Source Organon and Co
Contact
Status Completed
Phase Phase 3
Start date October 1, 2001
Completion date July 21, 2005
View Details
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