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

U

Universitaire Ziekenhuizen KU Leuven

Status

Completed

Conditions

Endometriosis

Study type

Observational

Funder types

Other

Identifiers

NCT01953250
S-54351

Details and patient eligibility

About

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

Full 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.

Enrollment

143 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

Trial design

143 participants in 1 patient group

Infiltrating endometriosis
Description:
272 patients that underwent laparoscopic sigmoid and/or rectum resection with the indication of deep infiltrating endometriosis, in the department of Abdominal Surgery, University Hospital Leuven, between the year 1997 and September 2011.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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