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

Endometriosis Clinical Trial

Official title:
To Assess the Functional Outcome in Patients That Underwent Laparoscopic Sigmoid and/or Rectum Resection

Clinical Trial Summary

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

Clinical Trial 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 Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01953250
Study type Observational
Source Universitaire Ziekenhuizen Leuven
Contact
Status Completed
Phase N/A
Start date June 2012
Completion date June 2013
View Details
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