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Completed Phase 3 Interventional

Efficacy and Safety of Topical Diclofenac Combined With Oral Diclofenac in the Treatment of Knee Osteoarthritis

ClinicalTrials.gov ID: NCT00108992

Public ClinicalTrials.gov record NCT00108992. 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, 4:00 AM EDT

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

Brief summary

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

Oral non-steroidal anti-inflammatory drugs (NSAIDs) are a recommended treatment for the symptoms of osteoarthritis of the knee. However, NSAIDs may cause a range of negative side effects, including stomach pain, heartburn, bleeding stomach ulcer, and liver or kidney abnormality. A topical NSAID may relieve pain and other symptoms of osteoarthritis of the knee, while minimizing the side effects common to oral NSAIDs. The purpose of this study is to determine the safety and effectiveness of a topical NSAID when used alone or when combined with an oral NSAID in the treatment of osteoarthritis of the knee.

Study identification

NCT ID
NCT00108992
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Nuvo Research Inc.
Industry
Enrollment
750 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
40 Years to 85 Years
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
Jan 31, 2004
Primary completion
Not listed
Completion
Aug 31, 2005
Last update posted
Jan 4, 2007

2004 – 2005

United States locations

U.S. sites
22
U.S. states
13
U.S. cities
22
Facility City State ZIP Site status
Coastal Clinical Research Mobile Alabama 36608
Redpoint Research Phoenix Arizona 85029
OMC Clinical Beverly Hills California 90211
Associated Pharmaceutical Research Buena Park California 90620
Med Investigators Fair Oaks California 95628
Desert Medical Advances Palm Desert California 92260
Boling Clinical Trials Upland California 91786
Tampa Bay Medical Research Inc. Clearwater Florida 33761
Palm Beach Research Center West Palm Beach Florida 33409
Medisphere Medical Research Evansville Indiana 47714
Synergy Medical Education Alliance Saginaw Michigan 48602
Redrock Research Center Las Vegas Nevada 89146
Partners in Primary Care Voorhees Township New Jersey 08043
Camp Hill Clinical Research Center Camp Hill Pennsylvania 17011
Primary Physicians Research Pittsburgh Pennsylvania 15241
University Orthopedics Center State College Pennsylvania 16801
Omega Medical Research Warwick Rhode Island 02886
Clinical Research Associates Nashville Tennessee 37203
Research Across America Dallas Texas 75234
Sam Clinical Research Center San Antonio Texas 78229
Hamptom Roads Center for Clinical Research Norfolk Virginia 23502-9921
National Clinical Research Richmond Virginia 23294

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 NCT00108992, 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 Jan 4, 2007 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00108992 live on ClinicalTrials.gov.

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