741845
Last Update Posted: 2012-03-06
Recruiting has ended
Females accepted | 18 Years-40 Years |
117 Estimated Participants | No Expanded Access |
Interventional Study | Does not accept healthy volunteers |
Prevention of Persistence of Bacterial Vaginosis
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.
Eligibility
Relevant conditions:
Bacterial Vaginosis
If you aren't sure if you meet the criteria above speak to your healthcare professional. Criteria may be updated but not reflected here, do not hesitate to contact the study if you think are close to fitting criteria.
locations
Data sourced from ClinicalTrials.gov