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Completed Phase 4 Interventional Accepts healthy volunteers

Comparison of Small Bowel Lesions Associated With Celecoxib Versus Ibuprofen Plus Omeprazole

ClinicalTrials.gov ID: NCT00640809

Public ClinicalTrials.gov record NCT00640809. 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 24, 2026, 2:16 AM EDT

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

Official title

Double-Blind, Placebo-Controlled, Randomized Two-Week Study, Comparing Small Bowel Lesions Associated With Celecoxib (200 mg BID) vs. Ibuprofen (800 mg TID) Plus Omeprazole (20 mg QD)

Brief summary

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

To evaluate the small bowel lesion pattern associated with celecoxib alone versus ibuprofen plus omeprazole

Study identification

NCT ID
NCT00640809
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
408 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2003 (Type not available)
Primary completion
Not listed
Completion
Apr 2004 (Actual)
Last update posted
Feb 2, 2021

2003 – 2004

United States locations

U.S. sites
12
U.S. states
8
U.S. cities
11
Facility City State ZIP Site status
Pfizer Investigational Site Scottsdale Arizona 85259 —
Pfizer Investigational Site La Jolla California 92037 —
Pfizer Investigational Site Los Angeles California 90033 —
Pfizer Investigational Site Los Angeles California 90073 —
Pfizer Investigational Site Jupiter Florida 33458 —
Pfizer Investigational Site Miami Florida 33173 —
Pfizer Investigational Site Chicago Illinois 60612 —
Pfizer Investigational Site Rockford Illinois 61107 —
Pfizer Investigational Site Ann Arbor Michigan 48109-0362 —
Pfizer Investigational Site New York New York 10021 —
Pfizer Investigational Site Portland Oregon 97239 —
Pfizer Investigational Site Nashville Tennessee 37232-5280 —

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 NCT00640809, 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 2, 2021 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00640809 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →