This observational study will evaluate treatment of symptomatic cystocele grade II-III with Cousin Biomesh and Allium Medical Endofast Reliant. Data about 100 patients will be collected. Follow-up till 3 years after the procedure. Primary endpoint is absence of recurrence.
Study Type
OBSERVATIONAL
Enrollment
100
RZ Heilig Hart Tienen
Tienen, Vlaams-Brabant, Belgium
Absence of recurrence
Time frame: 3 years
Technical success
Correct positioning of the mesh as intended by the surgeon
Time frame: day 1
Procedural success
Technical success without complications till 30 days after the index-procedure
Time frame: 30 days
Peroperative complications
Perforation bowels, bladder or arteries
Time frame: day 1
Postoperative complications
Infection, bleeding, recurrence, mesh erosion, pain during sexual activities, pain, discomfort
Time frame: 3 years
Quality of life
PFDI-20, PFIQ-7, PISQ-12
Time frame: 3 years
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