Clinical Trials Directory

Trials / Completed

CompletedNCT00576004

Pelvic Organ Prolapse Repair With or Without Concomitant Burch Colposuspension in Patients With Urinary Incontinence

Pelvic Organ Prolapse Repair With or Without Concomitant Burch Colposuspension in Patients With Urinary Incontinence: A Randomised Surgical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
67 (actual)
Sponsor
University Of Perugia · Academic / Other
Sex
Female
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

To evaluate the impact of Burch colposuspension (BC), as an anti-incontinence measure, in patients with urinary incontinence (UI) undergoing abdominal surgery for pelvic organ prolapse (POP) repair

Detailed description

Forty-seven women suffering from POP and UI were randomly assigned to abdominal POP repair and concomitant BC ( 24 patients; group A) or POP repair alone without any anti-incontinence procedure ( 23 patients.; group B). They were followed-up at 3, 6, and 9 months after surgery and then annually. The primary outcome measures were anatomical outcome and changes in incontinence status as indicated by a bladder diary, the number of daily pads and the stress test. Secondary endpoints were changes in subjective symptoms and Quality of Life (QoL) as measured by the Urogenital Distress Inventory (UDI-6) and the Impact Incontinence Quality of Life (IIQ-7) questionnaires.

Conditions

Interventions

TypeNameDescription
PROCEDUREPelvic organ prolapse repair and Burch colposuspensionAbdominal pelvic organ prolapse repair and retropubic Burch colposuspension

Timeline

Start date
2002-01-01
Completion
2006-12-01
First posted
2007-12-18
Last updated
2007-12-18

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT00576004. Inclusion in this directory is not an endorsement.