Functional Outcome in Patients That Underwent Laparoscopic Sigmoid and/or Rectum Resection

Completed

• Conditions: Endometriosis

• Registration Number: NCT01953250
• Lead Sponsor: Universitaire Ziekenhuizen KU Leuven

Brief Summary

Questionnaire To assess the functional outcome in patients that underwent laparoscopic sigmoid and/or rectum resection.

Detailed Description

A questionnaire will be sent to every patient by mail. The questionnaire that will be used is the COREFO questionnaire (ColoRectal Functional Outcome).

Depending on the amount of responses, we will try to make connections between peri-operative data and functional outcome after considerable period of follow-up. Peri-operative factors include grade of endometriosis, surgical technique and post-operative complications.

Study Timeline

• Status Verified: 2012-04
• Study Start: 2012-06
• Study First Submitted: 2013-02-19
• Primary Completion: 2013-06
• Study Completion: 2013-06
• Study First Submitted QC: 2013-09-25
• Last Update Submitted: 2013-09-25
• Study First Posted: 2013-09-30
• Last Update Posted: 2013-09-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 143

Inclusion Criteria

• Patients that underwent laparoscopic sigmoid and/or rectum resection with the indication of deep infiltrating endometriosis

Exclusion Criteria

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ColoRectal Functional Outcome	1 day	Operation: between 1997 and 2011 Questionnaire to assess the colorectal function sent once in 2012

Trial Locations

Locations (1)

University Clinics Gasthuisberg; 🇧🇪 Leuven, Flemish Brabant, Belgium