The Genital Microbiome of Male Partners of Women with Recurrent BV Undergoing Vaginal Microbiome Transplantation
NCT05963711 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100
Last updated 2025-03-19
Summary
There is strong observational evidence that sexual activity plays a key role in Bacterial Vaginosis (BV) acquisition and recurrence. Microbiological data support the contribution of sexual transmission to the pathogenesis of BV through the exchange of BV-associated bacteria (BVAB) between sexual partners.
Although BV epidemiology strongly suggests sexual transmission, treatment of sexual partners is not recommended, based on prior treatment studies of male partners of women with recurrent BV, which showed no benefit with male treatment. Nevertheless, male condom use is highly protective against recurrent BV.
This study aims to evaluate the male-partner's genital microbiome as a potential source of BV-recurrence in women undergoing vaginal microbiota transplantation (NCT04517487), and whether disinfection can eliminate BV-associated penile microbiome.
Conditions
- Bacterial Vaginosis
- Microbial Colonization
Interventions
- OTHER
-
chlorhexidine gluconate 4%
In case BV associated bacteria will be identified (using molecular sequencing) in male samples, decolonization attempt will be conducted, using a daily wash for 5 days with chlorhexidine gluconate 4%. Following decolonization attempt, male participants will undergo re- sampling, to assess for microbiome changes. In case there is no change in microbial composition, partners will be instructed to repeat decolonization protocol, and apply a 2 cm diameter volume of 2% clindamycin cream topically to the head of the penis and upper shaft (under the foreskin if uncircumcised) twice daily for seven days following repeated decolonization. Re-sampling will follow.
Sponsors & Collaborators
-
Hadassah Medical Organization
lead OTHER
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- MALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2022-10-17
- Primary Completion
- 2025-12-31
- Completion
- 2026-06-30
Countries
- Israel
Study Locations
More Related Trials
-
Safety and Efficacy of 5% Monolaurin Vaginal Gel Administered Intravaginally for the Treatment of Bacterial Vaginosis
NCT02709005 ·Status: COMPLETED ·Phase: PHASE2
-
Pathogenesis of Bacterial Vaginosis in Women Who Have Sex With Women
NCT02272231 ·Status: COMPLETED
-
Randomized Controlled Trial of Treatment of Male Partners of Women With BV
NCT02209519 ·Status: COMPLETED ·Phase: PHASE3
-
Bacterial Vaginosis; A Randomized Trial to Reduce Recurrence
NCT00542074 ·Status: COMPLETED ·Phase: NA
-
Efficacy of Two Vaginal Solutions in Preoperative Use
NCT03014778 ·Status: UNKNOWN ·Phase: PHASE4
-
Effect of Flourish HEC Vaginal Care System on BV Recurrence and the Vaginal Microbiome
NCT05701722 ·Status: COMPLETED ·Phase: NA
-
Study of UC-781 Vaginal Microbicide
NCT00132444 ·Status: COMPLETED ·Phase: PHASE1
-
Transplantation of Vaginal Mikrobiome
NCT04855006 ·Status: COMPLETED ·Phase: NA
-
GoldenCareTM for the Treatment of Bacterial Vaginosis
NCT01762670 ·Status: TERMINATED ·Phase: PHASE1/PHASE2
-
Clinical Study of a Vaginal Cooling Device for the Treatment of Vulvovaginal Candidiasis (VVC)
NCT06983041 ·Status: RECRUITING ·Phase: NA
-
Single Arm Trial of Menstrual Cups Among Economically Vulnerable Women to Reduce Bacterial Vaginosis and STIs
NCT05666778 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
Efficacy, Safety, and Dose-response of a Live Biotherapeutic Product in Women With Acute Vaginal Infection
NCT06450990 ·Status: NOT_YET_RECRUITING ·Phase: PHASE1/PHASE2
-
A Randomised, Partly-blinded Investigation to Evaluate the Clinical Performance and Safety of pHyph in Adult Women With Bacterial Vaginosis Compared With an Untreated Control Group
NCT06123299 ·Status: COMPLETED ·Phase: NA
-
Safety of Acidform Lubricant in HIV-Uninfected Women
NCT00850837 ·Status: COMPLETED ·Phase: PHASE1
-
Exploring the Effects of an Intravaginal Lactic Acid Gel on the Vaginal Microbiome
NCT05753813 ·Status: RECRUITING ·Phase: EARLY_PHASE1
-
Safety and Tolerability of Metronidazole Gel 1.3%
NCT02392026 ·Status: COMPLETED ·Phase: PHASE4
-
Evaluate the Safety of a Single Oral Dose of Solosec™ (Secnidazole) 2g for the Treatment of Adolescent Girls With BV
NCT03937869 ·Status: COMPLETED ·Phase: PHASE4
-
A Pilot Study to Evaluate the Efficacy and Safety of Lactobacillus Species Suppositories on Vaginal Health and pH
NCT05060029 ·Status: UNKNOWN ·Phase: PHASE4
-
Safety and Efficacy Study to Treat Bacterial Vaginosis
NCT01621399 ·Status: COMPLETED ·Phase: PHASE3
-
Chemoprevention of Cancer in the Lower Female Genital Tract: The Antineoplastic Activity of the Fungicide Ciclopirox.
NCT00382330 ·Status: WITHDRAWN ·Phase: NA
-
Effect of Bacterial Vaginosis on HIV Susceptibility and Female Genital Immunology
NCT02527941 ·Status: COMPLETED ·Phase: PHASE1
-
Multi-Center Study of New Medications to Treat Vaginal Infections
NCT02308033 ·Status: COMPLETED ·Phase: PHASE3
-
Multi-Center Study of New Medications to Treat Vaginal Infections
NCT02308046 ·Status: COMPLETED ·Phase: PHASE3
-
Safety, Tolerability and Efficacy of Vaginal Suppository WO3191 in the Post-treatment of Bacterial Vaginosis
NCT02687789 ·Status: COMPLETED ·Phase: NA
-
Safety and Efficacy of Boric Acid Inserts for Treatment of Vulvovaginal Candidiasis
NCT07109869 ·Status: RECRUITING ·Phase: PHASE3