Expired Study
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Cleveland, Ohio 44195


Purpose:

This is a registry-based observational study assessing clinical outcomes in FAP patients receiving celecoxib compared with historical/concurrent registry patients who have not received celecoxib. Both retrospective and prospective data will be utilized. No sampling methods apply.


Study summary:

The study prematurely discontinued on April 11, 2008 due to slow enrollment. It should be noted that safety concerns have not been seen in this study and have not factored into this decision.


Criteria:

Inclusion Criteria: Celecoxib Treated Patients: - Diagnosis of FAP based on the expression of the FAP phenotype. - Celecoxib treatment prescribed outside of a clinical trial setting with expected duration of celecoxib treatment of at least six months. Historical/Concurrent Control Patients: - Diagnosis of FAP based on the expression of the FAP phenotype. - Be greater than or equal to 12 years old at the time of study enrollment. - Have an endoscopically assessable colonic, rectal, ileal pouch and/or gastroduodenal segment. - For the group of post-surgical patients, IRA or IPAA performed from 1985 onward (in order to assure standardized surgical techniques and post-surgical management). Patients whose primary colorectal surgery was performed prior to 1985 will not be eligible to serve as historical controls. Exclusion Criteria: Celecoxib Treated Patients: - Have received a pharmacological treatment (other than celecoxib) within the last 3 months for their FAP disease including treatment of any extracolonic manifestation of FAP. - Have received a non-steroidal anti-inflammatory drug (NSAID) within the last 3 months, other than celecoxib, for any reason. Historical/Concurrent Control Patients: - Have pharmacological treatment recorded for their FAP disease at the defined index date. - Have received a non-steroidal anti-inflammatory drug (NSAID) within the last 3 months for any reason.


NCT ID:

NCT00151476


Primary Contact:

Study Director
Pfizer CT.gov Call Center
Pfizer


Backup Contact:

N/A


Location Contact:

Cleveland, Ohio 44195
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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