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NCT00549549 · ClinicalTrials.gov registry record · Phase 3

Celebrex In Acute Gouty Arthritis Study

A Phase 3 study, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.

Completed
Registry status
Phase 3
Development phase
402
Enrollment target

NCT00549549: Completed Phase 3 study, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.

NCT00549549 is a Phase 3 study that has completed, run by Pfizer's Upjohn has merged with Mylan to form Viatris. The registered enrollment target is 402 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (48% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00549549, a Phase 3 study, has completed, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.

COMPLETED
Registry status
Phase 3
Development phase
402 participants
Enrollment target

Study Summary

This is a multicenter, double-blind, double-dummy, randomized, active-controlled study that will include an 8-day treatment period followed by a 1-week follow-up period in patients experiencing symptoms of an acute exacerbation of gouty arthritis.

Primary Outcome

The Patient's Pain Intensity in the Index Joint for the prior 24 hours was assessed by completion of the following 5 point scale: My pain over the past 24 hours has been: None (0), Mild (1), Moderate (2), Severe (3), or Extreme (4).

Interventions

  • DRUG Celecoxib
  • DRUG Indomethacin

Trial Details

FieldValue
Enrollment Target 402 participants
Start Date 2008-02
Est. Completion 2009-12
Phase Phase 3

What the finished NCT00549549 record still lists

NCT00549549 is an interventional study that assigns participants to a tested intervention. The registered 402 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (48% lower).

The record links to 0 conditions, and to 2 interventions - of which Celecoxib is the first listed.

NCT00549549 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00549549 about?

NCT00549549 is a clinical study titled "Celebrex In Acute Gouty Arthritis Study". This is a multicenter, double-blind, double-dummy, randomized, active-controlled study that will include an 8-day treatment period followed by a 1-week follow-up period in patients experiencing symptoms of an acute exacerbation of gouty arthritis.

What is the current status of trial NCT00549549?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 402 participants. The study started on 2008-02. Estimated completion is 2009-12.

What interventions are being tested in trial NCT00549549?

The interventions under investigation include: Celecoxib (DRUG), Indomethacin (DRUG).

Who is sponsoring clinical trial NCT00549549?

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.

How this trial's enrollment target compares

Where NCT00549549's enrollment target sits among peer trials

402 919th of 2000 higher than 1,080 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00549549, the US trial registry maintained by the National Library of Medicine. NCT00549549 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.