A Multicenter Prospective Study of Posterior Transvaginal Mesh Compared to Native Tissue Repair for Pelvic Organ Prolapse: 36 Month Outcomes

Restorelle® DirectFix Posterior mesh demonstrated comparable efficacy and safety to NTR for treating posterior and apical compartment prolapse over a 36-month period. Clinical Trial Identification Number: NCT02162615. https://clinicaltrials.gov/study/NCT02162615. Registration date June 11, 2014.