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Terconazole Vaginal Suppository vs Fluconazole for the Treatment of Severe Vulvovaginal Candidiasis

Vulvovaginal Candidiasis Clinical Trial

Official title:
A Randomized, Parallel-group Study of Terconazole Vaginal Suppository vs Fluconazole for the Treatment of Severe

Clinical Trial Summary

The objectives of this study were to demonstrate comparable safety and efficacy of Terconazole Vaginal Suppositories, 80 mg and fluconazole in the treatment of subjects with severe vulvovaginal candidiasis.

Clinical Trial Description

This study were to demonstrate comparable safety and efficacy of Terconazole Vaginal Suppository 80 mg inserted intravaginally once daily before bedtime for 6 consecutive days and oral fluconazole 150mg at day 1 and day 4 in the treatment of subjects with severe vulvovaginal candidiasis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02180100
Study type Interventional
Source Peking University Shenzhen Hospital
Contact
Status Completed
Phase Phase 4
Start date August 2013
Completion date June 2014
View Details
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