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Completed Phase 3 Interventional Results available

5% Topical Ibuprofen (IBU) for Ankle Sprain

ClinicalTrials.gov ID: NCT01945034

Public ClinicalTrials.gov record NCT01945034. 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 Jul 21, 2026, 2:16 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

Placebo-controlled, Double-blind Evaluation Of The Efficacy And Safety Of Ibuprofen 5% Topical Gel For The Treatment Of Ankle Sprain

Study identification

NCT ID
NCT01945034
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
304 participants

Conditions and interventions

Conditions

Interventions

  • Topical IBU twice daily Drug
  • Placebo twice daily Drug
  • Topical IBU three times daily Drug
  • Placebo three times daily Drug

Drug

Eligibility (public fields only)

Age range
12 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
Oct 31, 2013
Primary completion
Jan 31, 2015
Completion
Jan 31, 2015
Last update posted
May 25, 2016

2013 – 2015

United States locations

U.S. sites
19
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Helen Keller Hospital Sheffield Alabama 35660
Visions Clinical Research - Tucson Tucson Arizona 85712
Orange County Research Institute Anaheim California 92801
eStudy Site San Diego California 92120
San Diego Sports Medicine and Family Health Center San Diego California 92120
Sunrise Research Institute, Inc. Miami Florida 33130
L&L Research Choices Miami Florida 33144
Doctors Research Network South Miami Florida 33143
Elite Clinical Trials LLLP Blackfoot Idaho 83221
MedPharmics, LLC Metairie Louisiana 70006
Quality Clinical Research, Inc. Omaha Nebraska 68114
Heartland Clinical Research, Inc. Omaha Nebraska 68134
PMG Research of Salisbury Salisbury North Carolina 28144
Lillestol Research, LLC Fargo North Dakota 58103
Clinical Trial Network Houston Texas 77074
Clinical Trials of Texas, Inc. San Antonio Texas 78229
Clinical Trials of Texas San Antonio Texas 78229
Sports Medicine Associates of San Antonio San Antonio Texas 78240
Danville Orthopedic Clinic Danville Virginia 24541

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 NCT01945034, 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 25, 2016 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01945034 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →