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NCT00633438 · ClinicalTrials.gov registry record · Phase 4
Effect of Celecoxib Versus Placebo Before and After Knee Surgery on Overall Use of Analgesics After Surgery
A Phase 4 study of Arthroscopy, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.
- Completed
- Registry status
- Phase 4
- Development phase
- 204
- Enrollment target
- 18
- Study locations
NCT00633438 is a Phase 4 study of Arthroscopy that has completed, run by Pfizer's Upjohn has merged with Mylan to form Viatris. The registered enrollment target is 204 participants. The trial reports 18 study locations across 8 states.
The verdict
NCT00633438, a Phase 4 study of Arthroscopy, has completed, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 204 participants
- Enrollment target
- 18
- Study locations
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
| Field | Value |
|---|---|
| Enrollment Target | 204 participants |
| Start Date | 2004-01 |
| Est. Completion | 2004-06 |
| Phase | Phase 4 |
Interested in This Trial?
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, categorized as Phase 4. 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 158 total studies on file at ClinicalTrials.gov.
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.
NCT00633438 reports 18 study locations spanning 8 distinct geographic areas - top geographies include Massachusetts, South Carolina, Texas.
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.
What interventions are being tested in trial NCT00633438?
The interventions under investigation include: Placebo (OTHER), Celecoxib (DRUG).
Who is sponsoring clinical trial NCT00633438?
This trial is sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris, which has 158 total clinical trials registered on ClinicalTrials.gov.
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.
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