The purpose of this study is to prospectively assess the outcomes of robotic sacrocolpopexy
for repair of pelvic organ prolapse in high volume european centers.
Procedure: Robotic assisted sacrocolpopexy (RASC)
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Full eligibility criteria for NCT01598467
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Symptomatic vaginal vault prolapse with simplified pelvic organ prolapse quantification (POP-Q) stage 2 or greater
Poor health status with inability to undergo general anaesthesia
Age < 18 years
≥ 3 previous laparotomic surgeries
Other: known pelvic malignancies, previous pelvic radiotherapy, congenital anomalies of genitourinary tract, autoimmune diseases with connective tissue involvement (Lupus, Sjogren Sdr, sclerodermia, etc.), current UTI's, use of steroids, anticoagulants, interstitial cystitis
All locations for NCT01598467
Cork University Maternity Hospital
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Tris trial is registered with FDA with number: NCT01598467. The sponsor of the trial is Femke van Zanten and it is looking for 300 volunteers for the current phase.
Official trial title: Prospective Interventional Study on Robotic Sacrocolpopexy: a European Multicentric Cohort (PARSEC)
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