CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 32 enrolled
Drug / intervention
Metronidazole +1 moredrug
Likely dose
Not stated in 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/NCT02042287
NCT02042287Phase 4Completed

Controlled, Multicenter, Randomized Parallel Group Pilot Study With 2 Treatment Arms in Non-pregnant Women With Acute Symptomatic Bacterial Vaginosis (BV)

Insel Gruppe AG, University Hospital Bern·interventional·Posted Jan 22, 2014·Updated Apr 8, 2022

In Brief

A Phase 4 clinical trial evaluating Vaginal lactic acid and glycogen gel and Metronidazole for Bacterial Vaginosis. Completed, enrolled 32 participants across 1 site.

Detailed Summary

Bacterial vaginosis (BV) is the most common cause of vaginitis in women of childbearing age. Women with symptomatic BV may present with malodorous discharge that is off-white, thin, and homogenous and has a fishy smell especially after intercourse. It is of importance to treat women with BV, as this condition is associated with serious risks, such as an increased risk of preterm birth in pregnant women, and particular vulnerability to the acquisition of sexually transmitted disease (STD). The pathophysiology of BV consists of changes in the microbiologic composition of the vaginal flora. The treatment of choice for BV is oral metronidazole for 7 days. Although the available antibiotic therapies produce good results in the short term, symptomatic BV persists or recurs at 3 months in up to 50% to 70% of patients, with long-term recurrence approaching 85%. An alternative treatment option may be a vaginal acid gel which aims to optimize the vaginal milieu. The aim of this pilot study is to assess the efficacy of Gynofit® vaginal gel (lactic acid and glycogen) compared to oral metronidazole in the treatment of BV.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesSwitzerland
CollaboratorsTentan AG

Timeline

Phase 4CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJan 22, 2014
Enrollment StartJun 1, 2014
Primary CompletionMar 19, 2020
TodayJul 2, 2026
Enrollment to primary: 5.8 yearsPosted 12.4 years ago

Interventions

Vaginal lactic acid and glycogen geldevice

Medical device (registration number: 10-355-717, first licensed 12.08.2010)

Metronidazoledrug

Oral antibiotic