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Completed Phase 3 Interventional

Double-Blind, Randomized Study Of The Analgesic Efficacy And Safety Of Valdecoxib 20 Mg Daily And Valdecoxib 20 Mg Twice Daily Compared To Placebo For Management Of Acute Postsurgical Pain In Anterior Cruciate Ligament (ACL) Reconstruction

ClinicalTrials.gov ID: NCT00650039

Public ClinicalTrials.gov record NCT00650039. 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 Oct 21, 2026, 3:43 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

A Multicenter, Double-Blind, Placebo-Controlled, Randomized Study Of The Analgesic Efficacy And Safety Of Valdecoxib 20 Mg QD And Valdecoxib 20 Mg BID Compared To Placebo Over Multiple Days For Management Of Acute Postsurgical Pain In Patients Undergoing Anterior Cruciate Ligament Reconstruction

Brief summary

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

The primary objective was to evaluate the analgesic efficacy of valdecoxib 20 mg daily and valdecoxib 20 mg twice daily compared with placebo in outpatients with moderate-severe pain after arthroscopic anterior cruciate ligament (ACL) reconstruction surgery. Secondary objectives were to compare each valdecoxib dose with placebo on additional measures of pain intensity, health outcomes, the use of rescue medication, and the occurrence of opioid-related symptoms, and to evaluate their safety.

Study identification

NCT ID
NCT00650039
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
488 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 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
Mar 2004 (Type not available)
Primary completion
Not listed
Completion
Feb 2005 (Actual)
Last update posted
Jun 4, 2008

2004 – 2005

United States locations

U.S. sites
68
U.S. states
17
U.S. cities
49
Facility City State ZIP Site status
Pfizer Investigational Site Birmingham Alabama 35205 —
Pfizer Investigational Site Birmingham Alabama 36205 —
Pfizer Investigational Site Northport Alabama 35476 —
Pfizer Investigational Site Glendale Arizona 85310 —
Pfizer Investigational Site Pheonix Arizona 85006 —
Pfizer Investigational Site Pheonix Arizona 85008 —
Pfizer Investigational Site Pheonix Arizona 85016 —
Pfizer Investigational Site Phoenix Arizona 85016 —
Pfizer Investigational Site Phoenix Arizona 85032 —
Pfizer Investigational Site Tempe Arizona 85281 —
Pfizer Investigational Site Glendale California 91206 —
Pfizer Investigational Site Laguna Hills California 92653 —
Pfizer Investigational Site Laguna Woods California 92653 —
Pfizer Investigational Site Los Angeles California 90045 —
Pfizer Investigational Site Avon Connecticut 06001 —
Pfizer Investigational Site Cromwell Connecticut 06416 —
Pfizer Investigational Site Enfield Connecticut 06082 —
Pfizer Investigational Site Farmington Connecticut 06030 —
Pfizer Investigational Site Farmington Connecticut 06032 —
Pfizer Investigational Site Glastonbury Connecticut 06033 —
Pfizer Investigational Site Hartford Connecticut 06102 —
Pfizer Investigational Site Hartford Connecticut 06106 —
Pfizer Investigational Site Rocky Hill Connecticut 06067 —
Pfizer Investigational Site Windsor Connecticut 06095 —
Pfizer Investigational Site Hollywood Florida 33021 —
Pfizer Investigational Site Jacksonville Florida 32216 —
Pfizer Investigational Site Jacksonville Florida 32250 —
Pfizer Investigational Site Plantation Florida 33324 —
Pfizer Investigational Site Saint Augustine Florida 32086 —
Pfizer Investigational Site St. Petersburg Florida 33703 —
Pfizer Investigational Site Weston Florida 33326 —
Pfizer Investigational Site Atlanta Georgia 30327 —
Pfizer Investigational Site Morrow Georgia 30260 —
Pfizer Investigational Site Stockbridge Georgia 30281 —
Pfizer Investigational Site Chicago Illinois 60304 —
Pfizer Investigational Site Chicago Illinois 60612 —
Pfizer Investigational Site Oak Park Illinois 60304 —
Pfizer Investigational Site Cedar Rapids Iowa 52401 —
Pfizer Investigational Site Lexington Kentucky 40504 —
Pfizer Investigational Site Lexington Kentucky 40509 —
Pfizer Investigational Site Baltimore Maryland 21218 —
Pfizer Investigational Site Timonium Maryland 21093 —
Pfizer Investigational Site Royal Oak Michigan 48073 —
Pfizer Investigational Site Troy Michigan 48085 —
Pfizer Investigational Site Springfield Missouri 65804 —
Pfizer Investigational Site Springfield Missouri 65807 —
Pfizer Investigational Site Las Vegas Nevada 89106 —
Pfizer Investigational Site Las Vegas Nevada 89117 —
Pfizer Investigational Site Las Vegas Nevada 89121 —
Pfizer Investigational Site Las Vegas Nevada 89144 —
Pfizer Investigational Site Bend Oregon 97701 —
Pfizer Investigational Site Anderson South Carolina 29621 —
Pfizer Investigational Site Cola South Carolina 29212 —
Pfizer Investigational Site Columbia South Carolina 29202 —
Pfizer Investigational Site Columbia South Carolina 29204 —
Pfizer Investigational Site Orangeburg South Carolina 29110 —
Pfizer Investigational Site Austin Texas 78705 —
Pfizer Investigational Site Dallas Texas 75231 —
Pfizer Investigational Site Fort Worth Texas 76104 —
Pfizer Investigational Site Fort Worth Texas 76107 —
Pfizer Investigational Site San Antonio Texas 78127 —
Pfizer Investigational Site San Antonio Texas 78209 —
Pfizer Investigational Site San Antonio Texas 78217 —
Pfizer Investigational Site San Antonio Texas 78229 —
Pfizer Investigational Site San Antonio Texas 78240 —
Pfizer Investigational Site San Marcos Texas 78666 —
Pfizer Investigational Site Arlington Virginia 22205 —
Pfizer Investigational Site Fairfax Virginia 22031 —

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 13 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00650039, 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 Jun 4, 2008 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00650039 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →