CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 25 enrolled
Drug / intervention
Prasterone 50 milligramdrug
Likely dose
Prasterone 50 milligramfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT07609043
NCT07609043Phase 3Completed

Impact of Prasterone on Cardiometabolic Indicators in Perimenopausal Women.

Universidad de Guanajuato·interventional·Posted May 27, 2026·Updated May 27, 2026

In Brief

A Phase 3 clinical trial evaluating Prasterone 50 milligram for Cardio Metabolic Risk. Completed, enrolled 25 participants across 1 site.

Detailed Summary

Perimenopause is the natural transition period towards menopause, in which the ovarian reserve begins to decrease, and the woman loses her fertility. It usually starts around the age of 40 and has a variable duration. It has been identified that the decrease in estrogen levels leads to the development of metabolic and cardiovascular complications, such as metabolic syndrome. Dehydroepiandrosterone (DHEA) is a hormone that converts to testosterone and estrogen and is mainly associated with age-related changes in cardiovascular tissues and metabolism, among others. This hormone declines with age, contributing to the development of age-related disorders, such as cardiovascular disease. In theory, DHEA has beneficial effects in regulating glucose and lipid metabolism and in ameliorating obesity. It is hypothesized that DHEAS and cardiovascular disease may share causal pathways, for example, nitric oxide synthesis and endothelial cell damage. In addition, it has been observed that the administration of DHEA significantly reduces the level of triglycerides and improves insulin sensitivity. There are few studies focused on the perimenopause stage and none of them focused on the prevention of cardiometabolic risk. Therefore, evaluating the impact of prasterone on cardiometabolic indicators in premenopausal women is essential.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesMexico
Collaborators--

Timeline

Phase 3CompletedFinished
2020202120222023202420252026
First PostedMay 27, 2026
Enrollment StartJan 10, 2020
Primary CompletionDec 20, 2020
Study CompletionJan 10, 2021
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 1 month ago

Interventions

Prasterone 50 milligramdrug

The participants were prescribed 50mg/day of prasterone for a period of 2 months, making 3 measurements (0, 4 and 8 weeks)