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Completed Phase 4 Interventional

Safety and Efficacy of Celecoxib Versus Naproxen in the 6-month Treatment of Knee Osteoarthritis

ClinicalTrials.gov ID: NCT00643799

Public ClinicalTrials.gov record NCT00643799. 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 9, 2026, 10:23 AM 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, Multicenter, Double-Blind, Double-Dummy Study Comparing the Efficacy and Tolerability of Once Daily Celebrex (Celecoxib) and Naproxen 500 mg Twice Daily in the 6-month Treatment of Subjects With Osteoarthritis of the Knee

Brief summary

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

To compare the safety and efficacy of celecoxib versus naproxen for the treatment of knee osteoarthritis

Study identification

NCT ID
NCT00643799
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
586 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
40 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 2004 (Type not available)
Primary completion
Jan 2005 (Actual)
Completion
Jan 2005 (Actual)
Last update posted
Feb 2, 2021

2004 – 2005

United States locations

U.S. sites
51
U.S. states
23
U.S. cities
44
Facility City State ZIP Site status
Pfizer Investigational Site Montgomery Alabama 36106 —
Pfizer Investigational Site Phoenix Arizona 85014 —
Pfizer Investigational Site Tempe Arizona 85282 —
Pfizer Investigational Site Buena Park California 90620 —
Pfizer Investigational Site Paramount California 90723 —
Pfizer Investigational Site Rancho Mirage California 92270 —
Pfizer Investigational Site San Diego California 92103 —
Pfizer Investigational Site San Diego California 92108 —
Pfizer Investigational Site Denver Colorado 80230 —
Pfizer Investigational Site Washington D.C. District of Columbia 20006 —
Pfizer Investigational Site Clearwater Florida 33761 —
Pfizer Investigational Site DeLand Florida 32720 —
Pfizer Investigational Site Jacksonville Florida 32204 —
Pfizer Investigational Site Miami Florida 33186 —
Pfizer Investigational Site Ocala Florida 34474 —
Pfizer Investigational Site Orlando Florida 32804 —
Pfizer Investigational Site Pembroke Pines Florida 33024 —
Pfizer Investigational Site Tampa Florida 33614 —
Pfizer Investigational Site Zephyrhills Florida 33542 —
Pfizer Investigational Site Rockford Illinois 61103 —
Pfizer Investigational Site Wichita Kansas 67207 —
Pfizer Investigational Site Wichita Kansas 67212 —
Pfizer Investigational Site Lexington Kentucky 40503 —
Pfizer Investigational Site Lexington Kentucky 40515 —
Pfizer Investigational Site Covington Louisiana 70433 —
Pfizer Investigational Site Metairie Louisiana 70006 —
Pfizer Investigational Site Clinton Maryland 20735 —
Pfizer Investigational Site Greenbelt Maryland 20770 —
Pfizer Investigational Site Hagerstown Maryland 21740 —
Pfizer Investigational Site Wheaton Maryland 20902 —
Pfizer Investigational Site Milford Massachusetts 01757 —
Pfizer Investigational Site Lansing Michigan 48910 —
Pfizer Investigational Site Flowood Mississippi 39232 —
Pfizer Investigational Site Kansas City Missouri 64114 —
Pfizer Investigational Site Lincoln Nebraska 68506 —
Pfizer Investigational Site Lincoln Nebraska 68516 —
Pfizer Investigational Site New York New York 10022 —
Pfizer Investigational Site Beachwood Ohio 44122 —
Pfizer Investigational Site Columbus Ohio 43124 —
Pfizer Investigational Site Columbus Ohio 43215 —
Pfizer Investigational Site Columbus Ohio 43222 —
Pfizer Investigational Site Oklahoma City Oklahoma 73103 —
Pfizer Investigational Site Bethlehem Pennsylvania 18015 —
Pfizer Investigational Site Duncansville Pennsylvania 16635 —
Pfizer Investigational Site Media Pennsylvania 19603 —
Pfizer Investigational Site Warwick Rhode Island 02886 —
Pfizer Investigational Site Austin Texas 78705 —
Pfizer Investigational Site Dallas Texas 75235 —
Pfizer Investigational Site San Angelo Texas 76904 —
Pfizer Investigational Site Salt Lake City Utah 84109 —
Pfizer Investigational Site Salt Lake City Utah 84121 —

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 NCT00643799, 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 Feb 2, 2021 · Synced Nov 9, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00643799 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →