Effects of Tibolone on the Endometrium in Postmenopausal Women
Data Collection
Bone Diseases+3
+ Bone Diseases, Metabolic
+ Metabolic Diseases
Treatment Study
Summary
Study start date: February 1, 2003
Actual date on which the first participant was enrolled.This study focuses on the effects of a medication called Tibolone on the endometrium, the lining of the uterus. Postmenopausal women often experience symptoms like hot flashes and bone loss due to a deficiency in estrogen. While estrogen treatment can help, it can also increase the risk of endometrial hyperplasia, a thickening of the endometrium that can lead to cancer. Tibolone is a unique compound that treats menopause symptoms and prevents bone loss without stimulating the endometrium like estrogens do. It's converted in the body into metabolites with estrogenic, progestagenic, and androgenic effects. The goal of this study is to understand Tibolone's effects on the endometrium, as it has been observed to cause a slight increase in thickness after long-term use, although hyperplasia rarely occurs. In this clinical trial, postmenopausal women undergoing vaginal hysterectomy for prolapse treatment are assigned to one of four groups: no hormonal treatment, Tibolone treatment, estrogen-only treatment, or estrogen plus progestagen treatment. The treatments are administered orally for 21 days prior to surgery. The investigators are blinded to the patient treatments during the analysis. The study measures the effects of Tibolone on the endometrium by evaluating hormone levels, histology, and gene expression in the endometrium and sera. The primary outcomes include biochemical evaluation of uterine tissue and sera, histologic evaluation of the endometrium, and molecular assessment of gene expression.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.35 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location