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A Randomised, Controlled Study of Bimesh, Pelvicol for Vaginal Wall Prolapse

Vaginal Prolapse Clinical Trial

Official title:
A Randomised, Controlled Study of Bimesh, Pelvicol for Vaginal Wall Prolapse

Clinical Trial 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.

Clinical Trial 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. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00442247
Study type Interventional
Source Roskilde County Hospital
Contact
Status Active, not recruiting
Phase N/A
Start date September 2004
Completion date December 2008
View Details
See also
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