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Multicenter Study of the Safety and Efficacy of NAFT-500 in Tinea Pedis

NCT00750139 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 707

Last updated 2013-04-26

Study results available
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Summary

A research study to compare the safety and effectiveness of an investigational medication called NAFT-500 to placebo, when used in subjects with tinea pedis (athlete's foot).

Conditions

  • Tinea Pedis
  • Athlete's Foot

Interventions

DRUG

NAFT-500

topical cream 1 application every day up to 4 weeks weeks

DRUG

Placebo 2-weeks

placebo cream 1 application every day for up to 4 weeks

DRUG

Naftin 1%

topical allylamine cream applied once a day for up to 4 weeks

DRUG

Placebo 4-weeks

topical placebo cream applied once a day for up to 4 weeks

Sponsors & Collaborators

  • Merz North America, Inc.

    lead INDUSTRY

Principal Investigators

  • Lawrence Parish, MD · Paddington Testing Company

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-08-31
Primary Completion
2009-08-31
Completion
2009-12-31

Countries

  • United States

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 NCT00750139 on ClinicalTrials.gov