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Completed Phase 3 Interventional Results available

Retapamulin Versus Placebo in Secondarily-Infected Traumatic Lesions (SITL)

ClinicalTrials.gov ID: NCT00684177

Public ClinicalTrials.gov record NCT00684177. 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 Nov 6, 2026, 6:20 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Multicenter, Placebo-controlled, Phase III Superiority Study to Assess the Safety and Efficacy of Topical Retapamulin Ointment, 1%, Versus Placebo Ointment Applied Twice Daily for 5 Days in the Treatment of Adult and Pediatric Subjects With SITL

Brief summary

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

The purpose of Study TOC110977 is to demonstrate clinical superiority of Retapamulin ointment, 1%, over placebo in patients with secondarily-infected traumatic lesions, which includes secondarily-infected lacerations, abrasions and sutured wounds. Subjects 2 months of age and older will be treated with topical retapamulin or placebo ointment twice daily for 5 days. The primary endpoint of this study is the clinical response at follow-up (Day 12-14; 7-9 days after the end of therapy) in the intent-to-treat clinical population.

Study identification

NCT ID
NCT00684177
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
508 participants

Conditions and interventions

Eligibility (public fields only)

Age range
2 Months 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
May 2008 (Type not available)
Primary completion
Oct 2009 (Actual)
Completion
Oct 2009 (Actual)
Last update posted
Nov 23, 2016

2008 – 2009

United States locations

U.S. sites
32
U.S. states
16
U.S. cities
30
Facility City State ZIP Site status
GSK Investigational Site Tucson Arizona 85705 —
GSK Investigational Site Anaheim California 92804 —
GSK Investigational Site Fresno California 93710 —
GSK Investigational Site Irvine California 90620 —
GSK Investigational Site Los Angeles California 90048 —
GSK Investigational Site Sacramento California 95825 —
GSK Investigational Site Colorado Springs Colorado 80904 —
GSK Investigational Site Deerfield Beach Florida 33441 —
GSK Investigational Site Hollywood Florida 33023 —
GSK Investigational Site Miami Florida 33144 —
GSK Investigational Site Miami Florida 33155 —
GSK Investigational Site Orlando Florida 32712 —
GSK Investigational Site Panama City Florida 32401 —
GSK Investigational Site Tampa Florida 33606 —
GSK Investigational Site Vero Beach Florida 32960 —
GSK Investigational Site West Palm Beach Florida 33401 —
GSK Investigational Site Arlington Heights Illinois 60005 —
GSK Investigational Site Kansas City Kansas 66160 —
GSK Investigational Site New Orleans Louisiana 70112 —
GSK Investigational Site Butte Montana 59701 —
GSK Investigational Site Teaneck New Jersey 07666 —
GSK Investigational Site Brooklyn New York 11218 —
GSK Investigational Site Brooklyn New York 11229 —
GSK Investigational Site East Syracuse New York 13057 —
GSK Investigational Site Johnson City New York 13790 —
GSK Investigational Site Cincinnati Ohio 45246 —
GSK Investigational Site Norristown Pennsylvania 19401 —
GSK Investigational Site Uniontown Pennsylvania 15401 —
GSK Investigational Site Greenville South Carolina 29615 —
GSK Investigational Site Houston Texas 77036 —
GSK Investigational Site Bountiful Utah 84010 —
GSK Investigational Site Vienna Virginia 22180 —

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 22 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00684177, 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 Nov 23, 2016 · Synced Nov 6, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00684177 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →