CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 17 enrolled
Drug / intervention
Leuprolide acetate +3 moredrug
Likely dose
Leuprolide acetate 3.75 mgfrom 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/NCT02122198
NCT02122198N/ACompleted

Vascular Mechanisms for the Effects of Loss of Ovarian Hormone Function on Cognition in Women

University of Colorado, Denver·interventional·Posted Apr 24, 2014·Updated Jan 10, 2022

In Brief

A clinical study evaluating Leuprolide acetate, Estradiol, and 2 other interventions for Cognitive Impairment and 3 related conditions. Completed, enrolled 17 participants across 2 sites.

Detailed Summary

Complaints about memory and thinking are common in women as they go through menopause and estrogen levels fall. The ovarian hormone estrogen is important for supporting normal cognitive function, and changes in brain activity and function occur when estrogen levels are decreased. Estrogen is also important for maintaining healthy blood vessels which also support normal cognitive function. In Alzheimer's disease and other types of dementia, there is significant damage to the blood vessels in the brain. This study will test whether changes in brain activity and function with the loss of estrogen are related to changes in vascular function. The investigators will measure vascular function using ultrasound, and brain activity using MRI scans in women who are enrolled in the Females, Aging, Metabolism and Exercise (FAME) study (NCT01712230). In the FAME study, healthy premenopausal women either take a medication to decrease their estrogen levels, or a placebo. This sub-study may provide new information about how estrogen affects vascular function and cognitive function, and lead to new ways to prevent or delay cognitive impairment or dementia.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedApr 24, 2014
Enrollment StartSep 8, 2014
Primary CompletionMay 30, 2017
Study CompletionSep 15, 2017
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 12.2 years ago

Interventions

Leuprolide acetatedrug

Lupron 3.75 mg for depot suspension delivered by monthly intramuscular injection for 9 months. First 6 months under parent study (FAME) protocol (NCT01712230); months 6-9 under sub-study.

Estradioldrug

Climara transdermal patch 0.075mg/day applied weekly months 6-9

Medroxyprogesteronedrug

Provera 5mg tablets once daily by mouth for 12 days beginning at week 30.

Placebodrug

placebo