NCT02209337View on ClinicalTrials.gov

Demonstrate the Safety and Preformance of the SRS Device for the Treatment of Pelvic Organ Prolapse

NACompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

September 30, 2014

Primary Completion Date

March 31, 2016

Study Completion Date

March 31, 2018

Conditions
Anterior Vaginal Wall ProlapseVaginal Apex/Uterine Prolapse
Interventions
DEVICE

SRS

Trial Locations (3)

51544

Mayanei HaYeshua Medical Center, Bnei Brak

70300

Asaf HaRofeh Medical Center, Zrifin

Unknown

University of Szeged, Szeged

Sponsors

Lead Sponsor

Lyra Medical Ltd.
All Listed Sponsors
lead

Lyra Medical Ltd.

INDUSTRY