Trials / Unknown
UnknownNCT00442247
A Randomised, Controlled Study of Bimesh, Pelvicol for Vaginal Wall Prolapse
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (planned)
- Sponsor
- Zealand University Hospital · Academic / Other
- Sex
- Female
- Age
- 55 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
Anterior vaginal wall prolapse is a common problem. Until now many different surgical techniques have been evaluated but so far recurrence is often still observed. Therefore, synthetic mesh or biomesh for vaginal prolapse reconstruction have been introduced.
Detailed description
Anterior vaginal wall prolapse is a common problem. Until now many different surgical techniques have been evaluated but so far recurrence is often still observed. Therefore, synthetic mesh or biomesh for vaginal prolapse reconstruction have been introduced. However, is is now known whether these methods are superior to the replication of the pubocervicale fascia, a method which is well described and have been used for many years. Furthermore, most studies evaluating the used of mesh for anterior vaginal wall prolapse have not been controlled studies and been irrespective to whether the repair was a primary or secondary operation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Pelvicol |
Timeline
- Start date
- 2004-09-01
- Completion
- 2008-12-01
- First posted
- 2007-03-01
- Last updated
- 2007-03-01
Locations
1 site across 1 country: Denmark
Source: ClinicalTrials.gov record NCT00442247. Inclusion in this directory is not an endorsement.