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Clinical Trials/NCT01604564
NCT01604564
Completed
Not Applicable

KOPOF Registry (Patients Characteristics, Operative Data, Postoperative Outcome, Functional Postoperative Recovery ) of Patients in Which a Pouch Has Been Created Due to Colitis Ulcerosa (CU) or Familial Adenomatous Polyposis(FAP)

Universitaire Ziekenhuizen KU Leuven1 site in 1 country207 target enrollmentStarted: May 2012Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
207
Locations
1
Primary Endpoint
Evaluation of postoperatieve recovery

Overview

Brief Summary

The purpose of this registry is to collect information about patients in which a pouch has been created to improve in the future the quality of the surgery of the pouch.

Detailed Description

To improve the quality of the surgery of the pouch created in CU and FAP patients, the following information will be collected: Patients Characteristics, Operative Data, Postoperative Outcome and Functional Postoperative Recovery.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Colitis Ulcerosa or Familial Adenomatous Polyposis Patients With IPAA

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Evaluation of postoperatieve recovery

Time Frame: 1 YEAR

STANDARD QUESTIONS AT 1, 3, 6 AND 12 MONTHS FU

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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