Multicenter, Prospective, Non-randomized, Single-arm, Interventional Study for the Evaluation of the Safety and Preformance of the SRS Device for the Treatment of Pelvic Organ Prolapse

NACompletedINTERVENTIONAL

Enrollment

Participants

Timeline

Start Date

March 31, 2016

Primary Completion Date

December 20, 2020

Study Completion Date

December 20, 2020

Conditions

Anterior Vaginal Wall Prolapse With/Without Apical/Uterine Descent

Interventions

DEVICE

SRS - Self Retaining Support system

Trial Locations (3)

Mayanei HaYeshua Medical Center, Bnei Brak

Asaf HaRofeh Medical Center, Zrifin

Ziv Medical center, Safed