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Completed Phase 3 Interventional

Prevention of Colorectal Sporadic Adenomatous Polyps (PRESAP)

ClinicalTrials.gov ID: NCT00141193

Public ClinicalTrials.gov record NCT00141193. 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 May 10, 2026, 10:31 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

Clinical Protocol For a Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of Celecoxib (SC-58635) In The Prevention of Colorectal Sporadic Adenomatous Polyps (PRESAP)

Study identification

NCT ID
NCT00141193
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
1,561 participants

Conditions and interventions

Interventions

  • Celecoxib Drug

Drug

Eligibility (public fields only)

Age range
30 Years and older
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 31, 2001
Primary completion
Apr 30, 2007
Completion
Apr 30, 2007
Last update posted
Aug 5, 2008

2001 – 2007

United States locations

U.S. sites
10
U.S. states
6
U.S. cities
8
Facility City State ZIP Site status
Pfizer Investigational Site San Diego California 92123
Pfizer Investigational Site San Kiego California 92123
Pfizer Investigational Site North Chicago Illinois 60064
Pfizer Investigational Site Oak Park Illinois 60304
Pfizer Investigational Site Baltimore Maryland 21229
Pfizer Investigational Site Baltimore Maryland
Pfizer Investigational Site Philadelphia Pennsylvania 19107-5244
Pfizer Investigational Site Philadelphia Pennsylvania 19107
Pfizer Investigational Site Houston Texas 77030
Pfizer Investigational Site Richmond Virginia 23249

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 96 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00141193, 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 Aug 5, 2008 · Synced May 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00141193 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →