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ProViS (Prolift+M and Vita Sexualis) Study — ProViS  

Pelvic Organ Prolapse Clinical Trial

Official title:
ProViS (Prolift+M TM and Vita Sexualis) Study

Clinical Trial Summary

Transvaginal meshes (TVM) are indicated for the treatment of pelvic organ prolapse (POP) where surgical intervention is necessary. Due to a potential risk of de novo dyspareunia, TVM are mainly used in postmenopausal women and in case of recurrent POP. PROLIFT+M (Trademark) is based on a highly flexible material which is partially absorbable. We suggest that PROLIFT+M has less impact on the vita sexualis than conventional TVM and could also be used for the treatment of younger and/or sexually active women. This study observes women who are routinely treated with PROLIFT+M with regard to their sexual function before and after the surgery. The hypothesis is that there is no worsening in vita sexualis with PROLIFT+M.

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01997996
Study type Observational
Source Cantonal Hospital of St. Gallen
Contact
Status Completed
Phase N/A
Start date May 2011
Completion date October 2013
View Details
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