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Vaginal Infection Study 2

NCT00694928 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 843

Last updated 2012-03-05

No results posted yet for this study

Summary

This study will evaluate the efficacy and safety of a vaginal product compared with that of another vaginal product in the treatment of vaginal infections.

Conditions

  • Vaginal Infection

Interventions

DRUG

clindamycin phosphate/butoconazole nitrate

semi-solid, single dose

DRUG

butoconazole nitrate

semi-solid, single dose

Sponsors & Collaborators

  • Lumara Health, Inc.

    lead INDUSTRY

Principal Investigators

  • Jim Joffrion · Lumara Health, Inc.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
16 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-05-31
Primary Completion
2009-11-30
Completion
2009-11-30

Countries

  • United States
  • India
  • Russia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00694928 on ClinicalTrials.gov