Clinical Trials Directory

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

TypeNameDescription
DEVICEPelvicol

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.