Bacterial Vaginoses

2

Review clinical trials related to Bacterial Vaginoses. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Multi-Gyn ActiGel Plus for Treatment of Bacterial Vaginosis

This is a randomized, double-blind, placebo-controlled clinical investigation. The objective of the study is to confirm the efficacy of Multi-Gyn ActiGel Plus to treat BV as compared to a placebo control. Treatment arm 1: Multi-Gyn ActiGel Plus Treatment arm 2: placebo gel Both the Multi-Gyn ActiGel Plus and the placebo will be applied twice a day for 7 consecutive days. Visit 2 will be performed at 3 weeks after start of treatment A phone call will take place, at 5 weeks after start of treatment for subject with clinical cure at Visit 2. The total duration per subject is estimated 5 weeks and the total study duration is 13 months. Sample size is 100 subjects per treatment arm.

Participants needed: 200
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: BioClin BVUpdated: Sep 29, 2025Locations: 1
Eligibility criteria

Women diagnosed with BV (3 out of 4 Amsel criteria positive, with at least prese... [+4]

Current clinically manifest of sexually transmitted gynecologically infection, g... [+11]

Status: Recruiting

Vaginal Microbiome Transplantation for Recurrent Bacterial Vaginosis

Vaginal Microbiome Transplantation (VMT) may be beneficial in treating the most severe cases of recurrent and antibiotics-nonresponsive cases of BV. Recently, we completed a preliminary study in which we treated patients with recurrent and antibiotics-non-responsive, intractable BV, with VMT from healthy donors \[Lev-Sagie, Nature Medicine 2019\]. Four VMT recipients in this preliminary study featured a significant improvement of both clinical symptoms and dysbiotic vaginal microbiome composition and function, which persisted over a long follow-up period, while one recipient featured a partial remission. The proposed study is designed as a placebo, randomized controlled trial, and is aimed to further assess whether VMT may serve as a viable option in symptomatic, intractable BV. In the suggested study, we plan to compare transplantation of: 1) vaginal fluid from healthy donors, and 2) autologous transplantation, of the patient's own vaginal fluid.

Participants needed: 100
Trial details
Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Hadassah Medical OrganizationUpdated: Mar 19, 2025Locations: 1
Eligibility criteria

Ages 18-50 [+3]

Pregnancy or a planned pregnancy in the upcoming year [+2]