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Completed Phase 4 Interventional

Effect of Celecoxib Versus Placebo Before and After Knee Surgery on Overall Use of Analgesics After Surgery

ClinicalTrials.gov ID: NCT00633438

Public ClinicalTrials.gov record NCT00633438. 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 3, 2026, 5:30 PM EST

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

Official title

A Double-Blind, Placebo-Controlled, Randomized Comparison Study of the Efficacy of Celebrex 400 mg Single Dose Pre and Celebrex 200 mg Post Ambulatory Arthroscopic Knee Surgery for Total Analgesic Use After Surgery

Brief summary

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

To compare total analgesic use at 24 hours after arthroscopic knee surgery in celecoxib-treated versus placebo-treated patients

Study identification

NCT ID
NCT00633438
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
204 participants

Conditions and interventions

Conditions

Interventions

Other · Drug

Eligibility (public fields only)

Age range
18 Years to 65 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 2004 (Type not available)
Primary completion
Not listed
Completion
Jun 2004 (Actual)
Last update posted
Feb 21, 2021

2004

United States locations

U.S. sites
18
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
Pfizer Investigational Site Phoenix Arizona 85023 —
Pfizer Investigational Site St. Petersburg Florida 33713 —
Pfizer Investigational Site Baltimore Maryland 21218 —
Pfizer Investigational Site Timonium Maryland 21093 —
Pfizer Investigational Site Springfield Massachusetts 01104 —
Pfizer Investigational Site Springfield Massachusetts 01107 —
Pfizer Investigational Site Springfield Massachusetts 01109 —
Pfizer Investigational Site Springfield Massachusetts 01199 —
Pfizer Investigational Site Springfield Missouri 65807 —
Pfizer Investigational Site Columbia South Carolina 29202 —
Pfizer Investigational Site Columbia South Carolina 29204 —
Pfizer Investigational Site Columbia South Carolina 29212 —
Pfizer Investigational Site Orangeburg South Carolina 29110 —
Pfizer Investigational Site Johnson City Tennessee 37601 —
Pfizer Investigational Site San Antonio Texas 78205 —
Pfizer Investigational Site San Antonio Texas 78209 —
Pfizer Investigational Site San Antonio Texas 78229 —
Pfizer Investigational Site San Antonio Texas 78240 —

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 NCT00633438, 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 21, 2021 · Synced Nov 3, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00633438 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →