Trials / Completed
CompletedNCT00752193
Safety and Efficacy of a Vaginally Administered Probiotic Lactobacilli Delivery System.
Safety and Efficacy of a Vaginally Administered Probiotic Lactobacilli Delivery System
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 206 (actual)
- Sponsor
- University Ghent · Academic / Other
- Sex
- Female
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to assess the safety and the efficacy of vaginally administered probiotic lactobacilli in combination with antibiotic therapy (metronidazole) in women with microbiologically defined bacterial vaginosis.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Probiotic lactobacilli | Probiotic lactobacilli in combination with antibiotic therapy |
| OTHER | Placebo | Placebo in combination with antibiotic therapy |
Timeline
- Start date
- 2008-10-01
- Primary completion
- 2015-12-01
- Completion
- 2015-12-01
- First posted
- 2008-09-15
- Last updated
- 2021-11-19
Locations
1 site across 1 country: Belgium
Source: ClinicalTrials.gov record NCT00752193. Inclusion in this directory is not an endorsement.