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Laparoscopic Surgery for Severe Recto-vaginal Endometriosis

R

Royal Surrey County Hospital NHS Foundation Trust

Status

Enrolling

Conditions

Endometriosis Rectovaginal Septum

Treatments

Procedure: Surgery for severe endometriosis

Study type

Observational

Funder types

Other

Identifiers

NCT02471443
15DEV0009

Details and patient eligibility

About

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

Full 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.

Enrollment

1,000 estimated patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All women undergoing planned surgery for severe endometriosis with bowel involvement.

Exclusion criteria

  • Patients who declined to complete questionnaires for whatever reason and/or have their anonymous data analysed.

Trial design

1,000 participants in 1 patient group

Surgery for severe endometriosis
Description:
Consecutive patients undergoing excisional surgery for severe endometriosis with bowel involvement
Treatment:
Procedure: Surgery for severe endometriosis

Trial contacts and locations

1

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Central trial contact

Andrew Kent, TD MD FRCOG

Data sourced from clinicaltrials.gov

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