Prevention of Persistence of Bacterial Vaginosis

Status Terminated

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00741845
Study type	Interventional
Source	Embil Pharmaceutical Co. Ltd
Contact
Status	Terminated
Phase	Phase 3
Start date	June 2008

View Details

See also
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