Robotic removal of transvaginal mesh for pelvic organ prolapse and stress urinary incontinence

Not Applicable

Recruiting

• Conditions: Mesh complication; Pelvic pain; Urinary incontinence; Surgery - Surgical techniques; Renal and Urogenital - Other renal and urogenital disorders

• Registration Number: ACTRN12619000570189
• Lead Sponsor: rology institute

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-04-11
• Last Update Posted: 31 August 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 15

Inclusion Criteria

Women, 18 and over, with pelvic mesh and symptoms of mesh
complications (pain/ dyspareunia/ voiding symptoms/ mesh extrusion)

Exclusion Criteria

. Patients who have
previously had surgical mesh removal attempted will not be offered participation in this early phase
study but may be offered such an approach in subsequent work.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
- complete removal of mesh as measured in cms of mesh removed<br><br>[Post-operatively 0-10 days- documented by measurement in theatre, photograph and sent to laboratory for histological analysis and measurement of removed mesh , in cm. <br>]

Secondary Outcome Measures

Name	Time	Method
Change in pelvic pain measured by validated pain questionnaires: McGill Questionnaire, Female NIH- CPSI pain questionnaire, PILL. (composite secondary outcome) <br>[6 weeks, 1 year, 2 years, 5 years. ]