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COMPLETED Phase 4

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

NCT00633438 · View on ClinicalTrials.gov ↗

Study Summary

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

Conditions Studied

Interventions

  • OTHER Placebo
  • DRUG Celecoxib

Study Locations (18)

Massachusetts

  • Pfizer Investigational Site — Springfield
  • Pfizer Investigational Site — Springfield
  • Pfizer Investigational Site — Springfield
  • Pfizer Investigational Site — Springfield

South Carolina

  • Pfizer Investigational Site — Columbia
  • Pfizer Investigational Site — Columbia
  • Pfizer Investigational Site — Columbia
  • Pfizer Investigational Site — Orangeburg

Texas

  • Pfizer Investigational Site — San Antonio
  • Pfizer Investigational Site — San Antonio
  • Pfizer Investigational Site — San Antonio
  • Pfizer Investigational Site — San Antonio

Maryland

  • Pfizer Investigational Site — Baltimore
  • Pfizer Investigational Site — Timonium

Arizona

  • Pfizer Investigational Site — Phoenix

Florida

  • Pfizer Investigational Site — St. Petersburg

Missouri

  • Pfizer Investigational Site — Springfield

Tennessee

  • Pfizer Investigational Site — Johnson City

Trial Details

FieldValue
Enrollment Target 204 participants
Start Date 2004-01
Est. Completion 2004-06
Phase Phase 4

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00633438

The ClinicalTrials.gov registry entry for NCT00633438 describes a study currently listed as completed. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 204 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer's Upjohn has merged with Mylan to form Viatris, which has 27 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Arthroscopy appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00633438 reports 18 study locations spanning 8 distinct geographic areas — top geographies include Massachusetts, South Carolina, Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00633438 about?

NCT00633438 is a clinical study titled "Effect of Celecoxib Versus Placebo Before and After Knee Surgery on Overall Use of Analgesics After Surgery". To compare total analgesic use at 24 hours after arthroscopic knee surgery in celecoxib-treated versus placebo-treated patients

What is the current status of trial NCT00633438?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 204 participants. The study started on 2004-01. Estimated completion is 2004-06.

What conditions does trial NCT00633438 study?

This clinical trial studies the following conditions: Arthroscopy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00633438?

The interventions under investigation include: Placebo (OTHER), Celecoxib (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00633438?

This trial is sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris, which has 27 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00633438 being conducted?

This trial has 18 study locations across Arizona, Florida, Maryland, Massachusetts, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial