sing the Gynecare MoniTorr* device to measure urethral pressure before incontinence surgery

Not Applicable

Recruiting

• Conditions: rethral pressure; Urethral pressure; Renal and Urogenital - Other renal and urogenital disorders; Surgery - Other surgery

• Registration Number: ACTRN12605000182695
• Lead Sponsor: Johnson & Johnson Medical

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2005-08-19
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

Women with urodynamics stress incontinence undergoing a TVT procedure at the two study centres. Concomitant prolapse surgery is not a contraindication. Willingness to participate.

Exclusion Criteria

Medically unfit for surgery. Refusal to participate. Patients who are recommended surgery other than TVT (e.g. Colposuspension, Sling, Bulking agent, Transobturator procedure).

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
rodynamic stress incontinence[At 6 months after surgery]

Secondary Outcome Measures

Name	Time	Method
Visual analogue scale of patient satisfaction[];Bladder diary[]