Viewing Study NCT04079218



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Last Modification Date: 2024-10-26 @ 1:17 PM
Study NCT ID: NCT04079218
Status: COMPLETED
Last Update Posted: 2024-02-02
First Post: 2019-09-03

Brief Title: Accelerated Genital Tract Aging in HIV Estradiol Clinical Trial
Sponsor: Albert Einstein College of Medicine
Organization: Albert Einstein College of Medicine

Study Overview

Official Title: The Impact of HIV on Accelerated Aging in the Female Genital Tract a Pilot Trial of Topical Estradiol to Improve the Vaginal Microbiome and Symptoms of Vaginal Atrophy in Menopausal Women With HIV
Status: COMPLETED
Status Verified Date: 2024-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: During menopause there is a decrease in a hormone estrogen which leads to aging of the vagina Vaginal aging includes changes in the type and amount of healthy bacteria in the vagina inflammation and a breakdown of natural barriers that keep the vagina healthy and protected from infections Some menopausal women develop a condition called vaginal atrophy which causes vaginal dryness irritation pain with sex and itching We are testing whether an estradiol tablet placed inside the vagina will lead to fewer changes in the types of bacteria present in the vagina improve vaginal atrophy symptoms and ultimately keep the vagina healthier for a longer This is important for women with HIV as they are living longer healthier sexually active lives due to successful treatment with antiretrovirals
Detailed Description: HIV may be associated with premature aging in the female genital tract including alterations in the vaginal microbiome and mucosal inflammation which may increase risk for vaginal atrophy urinary tract infections UTI and other genital tract infections This study will determine whether use of vaginal estradiol for 12 weeks in menopausal women living with HIV with symptomatic vaginal atrophy will improve atrophy symptoms and the vaginal microbiome and reduce mucosal inflammation thereby improving vaginal health This study will include 50 participants randomized to treatment with a vaginal estradiol insert or no therapy for 12 weeks and will have 4 study visits

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: True
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
1K23AG062400-01A1 NIH None httpsreporternihgovquickSearch1K23AG062400-01A1