Tinea Pedis Clinical Trial
Official title:
A Randomized, Multi-Center, Double-Blind, Vehicle-Controlled Study Evaluating the Efficacy and Safety of Product 33525 in Subjects With Tinea Pedis
The purpose of this study is to determine if a topical antifungal cream is safe and effective for the treatment of tinea pedis.
Status | Completed |
Enrollment | 322 |
Est. completion date | March 2012 |
Est. primary completion date | January 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 12 Years and older |
Eligibility |
Inclusion Criteria: - Moderate erythema, moderate scaling, and mild pruritus Exclusion Criteria: - Pregnancy and allergies |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Medicis Global Service Corporation |
United States, Belize,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportion of patients achieving complete clearance | Signs and Symptoms Severity Score and negative Potassium Hydroxide (KOH) and Culture | Day 42 | No |
Secondary | Proportion of patients achieving effective treatment | Clinical Cure and Mycologic Cure | Day 42 | No |
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