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Clinical Trial Summary

To determine the quality of life following the radical excision of recto-vaginal endometriosis.


Clinical Trial Description

Patients undergoing surgery for severe endometriosis with bowel involvement were asked to complete pre-operative and post operative questionnaires at 2, 6 and 12 months, then 5, 10, 15, 20 and 25 years post operatively.

Quality of life measured using the EHP-30 and EQ-5D questionnaires. Bowel symptoms were measured using GIQLI. Dysmenorrhoea, dyspareunia, dyschezia and chronic pain were measured using a visual analogue scale. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02471443
Study type Observational
Source Royal Surrey County Hospital
Contact Andrew Kent, TD MD FRCOG
Email kenta@doctors.org.uk
Status Recruiting
Phase
Start date May 2004
Completion date January 2040

See also
  Status Clinical Trial Phase
Active, not recruiting NCT04171297 - Ultrasound Evaluation of the Pelvis in Women With Suspected Endometriosis Scheduled for Laparoscopic Surgery
Not yet recruiting NCT04401592 - The Role of Galectins in the Non-invasive Diagnosis of Endometriosis
Completed NCT04296760 - Rectal Water-contrast Transvaginal Ultrasonography Versus Sonovaginography for the Diagnosis of Posterior Deep Pelvic Endometriosis