Home › Bacterial Vaginosis › NCT05753813
Exploring the Effects of an Intravaginal Lactic Acid Gel on the Vaginal Microbiome
RecruitingEarly phase 1Healthy volunteers welcome
Who can join
Ages 18 to 54 · Women · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Age 18-54 * Female * Pre-menopausal * Can speak and read in English * Displays capacity for informed consent * Has had 2 or more documented and/or self-reported episodes of symptomatic BV or candida infection in the last year, requiring, over-the-counter or prescription treatment Exclusion Criteria: * Pregnant or trying to become pregnant * Post-menopausal * Using NuvaRing device * A past medical history of kidney disease, recurrent UTI, and/or urinary tract abnormalities * Current UTI * Using Phexxi as a contraceptive during the collection period of the study
About the study
This project aims to investigate if the contraceptive method, Phexxi, causes changes to the composition of the vaginal microbiome. The investigators hypothesize that regular use of Phexxi will cause increased colonization of lactic acid-producing lactobacilli, which could have positive effects in the way of preventing recurrent episodes of BV and candida infections.
What is being tested
- Phexxi (drug)
Sponsor: Queen's Medical Center · Participants: 22 · Started: Dec 15, 2023
Contact the study team
- Olivia H Manayan, MD, MPH · Phone: 808-348-7859
Official record on ClinicalTrials.gov — NCT05753813
Locations in the U.S.
| Hawaii | Queens Medical Center, 1004 Clinic POB1, Honolulu |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.