Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional

BE Study of Naftifine HCL

ClinicalTrials.gov ID: NCT02633813

Public ClinicalTrials.gov record NCT02633813. 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 Oct 18, 2026, 11:49 AM 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 Randomized, Prospective Multicenter, Double Blind, Parallel Assignment Placebo Controlled BE Study Of Naftifine Hydrochloride 2% Topical Cream With Naftin® In Patients With Tinea Pedis Using Clinical Endpoints

Brief summary

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

The current study was randomized, double blind, placebo-controlled, prospective, multicenter, comparative therapeutic equivalence study. The study duration for each patient was 6 weeks: Following were the visit details. V1-Baseline and Randomization Visit (Day 1). V2- End of therapy visit (at the end of week 2 + 2 days). V3- Follow up visit (at the end of week 4 + 2 days). V4 - Test of cure visit ( at the end of week 6 + 4 days).

Study identification

NCT ID
NCT02633813
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Genzum Life Sciences
Industry
Enrollment
693 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Mar 2015 (Type not available)
Primary completion
Nov 2015 (Actual)
Completion
Dec 2015 (Actual)
Last update posted
May 11, 2017

2015

United States locations

U.S. sites
12
U.S. states
3
U.S. cities
9
Facility City State ZIP Site status
Moore Clinical Research Inc Brandon Florida 33511 —
Savin Medical Group Research Miami Florida 33014 —
International Dermatology Research, Inc, Miami Florida 33144 —
FXM Research Corp Miami Florida 33175 —
FXM Research Miramar Miramar Florida 33027 —
South Tampa, MOORE Clinical Research, Inc. Tampa Florida 33609 —
North Tampa MOORE Clinical Research, Inc. Tampa Florida 33618 —
Medi Search Saint Joseph Missouri 64506 —
Bellaire Dermatology Associates Bellaire Texas 77401 —
Research Across America Dallas Texas 75234 —
Family Practise Mesquite Texas 75149 —
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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02633813, 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 May 11, 2017 · Synced Oct 18, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02633813 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →