Clinical Trials Directory

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

TypeNameDescription
DRUGintravaginal metronidazolehigh 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.

Prevention of Persistence of Bacterial Vaginosis (NCT00741845) · Clinical Trials Directory