Trials / Terminated
TerminatedNCT00741845
Prevention of Persistence of Bacterial Vaginosis
Prevention of Persistence of Bacterial Vaginosis: The Effects of High Dose Intravaginal Metronidazole
- Status
- Terminated
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 117 (actual)
- Sponsor
- Embil Pharmaceutical Co. Ltd · Industry
- Sex
- Female
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Not accepted
Summary
This purpose of this study will be to conduct a double-blind, randomized, controlled clinical trial to determine the association between intravaginal high dose metronidazole (750mg), intravaginal high dose metronidazole combined with an antifungal agent(750mg metronidazole + 200mg miconazole) and low dose (37.5mg) intravaginal metronidazole, with the rate of persistent bacterial vaginosis.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | intravaginal metronidazole | high dose intravaginal metronidazole 750mg (with or without miconazole) to be compared to low dose intravaginal metronidazole 37.5mg |
Timeline
- Start date
- 2008-06-01
- Primary completion
- 2009-06-01
- First posted
- 2008-08-26
- Last updated
- 2012-03-06
Locations
1 site across 1 country: Peru
Source: ClinicalTrials.gov record NCT00741845. Inclusion in this directory is not an endorsement.