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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Pelvic organ prolapse repair and Burch colposuspension | Abdominal 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.