A randomised trial comparing two vaginal prolene sling surgeries for female urinary incontinence

Not Applicable

Recruiting

• Conditions: stress urinary incontinence; Surgery - Surgical techniques; suburethral sling surgery

• Registration Number: ACTRN12612000314820
• Lead Sponsor: Dr Andrew Foote

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-03-20
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 50

Inclusion Criteria

no other surgery required, females only ages 16 - 90, urodynamically proven stress incontinence & fit for surgery

Exclusion Criteria

prolapse, detrusor overactivity or voiding difficulty, unit for surgery

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
post operative pain relief, assessed by pain scoring on a visual analogue scale from 0 to 10[4 hours post operatively];continence, assessed by bladder diaries over 2 days and clinical examination[2 day bladder diary and clinical examination at 6 months]

Secondary Outcome Measures

Name	Time	Method
blood loss, assessed by surgeons assessment[intraoperatively]