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Completed Phase 3 Interventional Accepts healthy volunteers Results available

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

ClinicalTrials.gov ID: NCT00750139

Public ClinicalTrials.gov record NCT00750139. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 6:39 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3 Double-Blind, Randomized, Placebo-Controlled, Multicenter, Parallel Group Evaluation of the Efficacy and Safety of NAFT-500 in Subjects With Tinea Pedis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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).

Study identification

NCT ID
NCT00750139
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Merz North America, Inc.
Industry
Enrollment
707 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 31, 2008
Primary completion
Jul 31, 2009
Completion
Nov 30, 2009
Last update posted
Apr 25, 2013

2008 – 2009

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Radiant Research Birmingham Alabama 35209
Dr. Felix Sigal Los Angeles California 90010-3209
University of California San Francisco, Dept of Dermatology San Francisco California 94115
FXM Research Miami Florida 33175
FXM Research Miramar Florida 33027
Glazer Dermatology Buffalo Grove Illinois 60089
Tulane University Health Services New Orleans Louisiana 70112
Silverton Skin Institute Grand Blanc Michigan 48439
Zoe Draelos, MD High Point North Carolina 27262
Haber Dermatology Euclid Ohio 44118
Oregon Dermatology and Research Center Portland Oregon 97210
Paddington Testing Company Philadelphia Pennsylvania 19103
Temple University School of Podiatric Medicine Philadelphia Pennsylvania 19107
Coastal Carolina Research Center Mt. Pleasant South Carolina 29464
J & S Studies College Station Texas 77845
Research Across America Dallas Texas 75234
Research Across America Plano Texas 75093

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00750139, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 25, 2013 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00750139 live on ClinicalTrials.gov.

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