OPUS F12 Follow Up Visit in Outcomes Following Vaginal Prolapse Repair and Mid Urethral Sling Trial

Data from the 2wk, 4-6 wk, 3m, 6m, 9m, 12m and other follow up visits [CRF 12]
Study Description
The overall objective of this study is to determine whether symptom-specific treatment of incontinence after prolapse surgery is equally effective to prophylactic treatment by adding TVT® at the time of the prolapse surgery among women with anterior vaginal prolapse but without pre-operative symptoms of stress urinary incontinence. Adult and senior women undergoing vaginal surgery for prolapse who have anterior vaginal prolapse but who do not have overt symptoms of stress urinary incontinence.