Clinical Research Directory

Inclusion Criteria: * Surgery for POP * Implantation of either EndoGYNious or PelviGYNious * Concomitant procedures are allowed * Women minimum 18 years old * Written informed consent for surgery Exclusion Criteria: Patients who rule out subsequent contact by the hospital will be excluded. The use of the products is contraindicated in case of: * pregnancy and/or patients who consider future pregnancies * adolescent/ pubescent patients * existence of a known sensitivity/ allergy against plastic materials such as polypropylene, polyester, etc. * any pathology, including known or suspected uterine pathology, which would compromise placement of the implant/mesh (e.g. anatomical distortion or abnormalities) * known anticoagulation disorder * anticoagulant therapy * autoimmune connective tissue disease * renal insufficiency and upper urinary tract obstruction * cancer illnesses of the vagina / cervix / rectum * undergone radiation therapy on the vagina, cervix, rectum * planned or emergency opening of the gastro-intestinal tract, as this could cause a risk of product contamination that could lead to infection that would require removal of the implant/device * active or latent infection especially of the genital system and/or urinary tract