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Completed Phase 4 Interventional Accepts healthy volunteers

Pediatric Subjects With Tinea Corporis

ClinicalTrials.gov ID: NCT02227290

Public ClinicalTrials.gov record NCT02227290. 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 5, 2026, 12:05 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 Phase 4, Double-Blind, Randomized, Vehicle-Controlled, Multicenter, Parallel Group Evaluation of the Efficacy and Safety of Naftin (Naftifine Hydrochloride) Cream, 2% in Pediatric Subjects With Tinea Corporis

Brief summary

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

The study is being done to see how well the study cream works when applied once a day to affected area of child (where they have ringworm). The results will be compared to those seen with a placebo cream which has no active ingredient. Safety of the cream will also be measured.

Study identification

NCT ID
NCT02227290
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Merz North America, Inc.
Industry
Enrollment
230 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
2 Years to 17 Years
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, 2014
Primary completion
Oct 31, 2015
Completion
Nov 30, 2015
Last update posted
Oct 27, 2016

2014 – 2015

United States locations

U.S. sites
14
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
Merz Investigative Site#001316 Tucson Arizona 85712
Investigative Site# 0010320 Encino California 91436
Merz Investigative Site#001313 Fremont California 94538
Merz Investigative Site#001301 San Diego California 92102
Merz Investigative Site#001312 Miami Florida 33144
Merz Investigative Site#001311 Miami Florida 33175
Merz Investigative Site #001310 Miramar Florida 33027
Merz Investigative Site#001307 Saint Joseph Missouri 64506
Merz Investigative Site#001309 Omaha Nebraska 68114
Merz Investigative Site#001314 Henderson Nevada 89074
Merz Investigative Site#001126 Raleigh North Carolina 27612
Merz Investigative Site#001293 Winston-Salem North Carolina 27104
Investigative Site# 0010319 Gresham Oregon 97030
Merz Investigative Site#001097 Nashville Tennessee 37215

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02227290, 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 Oct 27, 2016 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02227290 live on ClinicalTrials.gov.

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