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RecruitingNCT02471443

Laparoscopic Surgery for Severe Recto-vaginal Endometriosis

Laparoscopic Surgery for Severe Recto-vaginal Endometriosis: A Prospective Cohort Study

Status
Recruiting
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
Royal Surrey County Hospital NHS Foundation Trust · Academic / Other
Sex
Female
Age
Healthy volunteers
Accepted

Summary

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
PROCEDURESurgery for severe endometriosisConsecutive patients undergoing excisional surgery for severe endometriosis with bowel involvement

Timeline

Start date
2004-05-01
Primary completion
2025-01-01
Completion
2040-01-01
First posted
2015-06-15
Last updated
2019-03-26

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT02471443. Inclusion in this directory is not an endorsement.

Laparoscopic Surgery for Severe Recto-vaginal Endometriosis (NCT02471443) · Clinical Trials Directory