Performance of Tension Free Vaginal Mesh (Prolift) Versus Conventional Vaginal Prolapse Surgery in Recurrent Prolapse.

Patients with recurrent prolapse after surgery can participate in this study. A total of 194 women will be included. At random 97 patients undergo a standard prolapse operation and 97 patients undergo an operation with the mesh. Evaluation will take place during surgery, at the postoperative visit after six weeks, and after six months and twelve months. Quality of life, degree of vaginal prolapse, subjective effectiveness, safety and incidence of complications will be evaluated.

An amendment to the original study has been approved by the Ethical Committee to examine long term outcome of this RCT at 7 years. This study was completed in december 2015.

Inclusion criteria

• recurrent anterior and/or posterior prolapse POP-Q stage 2 or more
• patient has agreed to undergo implantation of TVM (prolift) or fascial plication
• patient is willing to return for follow-up evaluation at 6 weeks, 6 months and 12 months
• patient is willing to complete quality of life questionnaires at 6 and 12 months

Exclusion criteria

• patient is or wants to become pregnant
• patient has had previous synthetic mesh procedure (a previous mid-urethral sling procedure is NOT an exclusion criterion)
• patient has current urinary tract or vaginal infections
• patient has a blood coagulation disorder
• patient has a compromised immune system or any other condition that would compromise healing
• patient has renal insufficiency and/or upper urinary tract obstruction
• patient is unwilling or unable to return for evaluation
• patient has had previous irradiation
• patient has any malignancy
• patient has large ovarian cysts of large myoma