NCT00557882View on ClinicalTrials.gov

Efficacy Study of Vaginal Mesh for Anterior Prolapse

PHASE4CompletedINTERVENTIONAL
Enrollment

65

Participants

Timeline

Start Date

June 30, 2007

Primary Completion Date

October 31, 2009

Study Completion Date

November 30, 2011

Conditions
Vaginal ProlapseUterine ProlapseCystocelePelvic Organ Prolapse
Interventions
DEVICE

synthetic polypropylene mesh

Mesh used will be synthetic monofilament polypropylene. In this trial, patients in the experimental group will undergo interpositional multi-armed mesh placement using trocars for transobturator +/- ischioanal fossa placement at the level of the ischial spine.

Trial Locations (1)

20010

Wahington Hospital Center, Washington D.C.

Sponsors
All Listed Sponsors
lead

Medstar Health Research Institute

OTHER