Geneva, May 4 -- International Clinical Trials Registry received information related to the study (ACTRN12626000496314) titled 'Robot-Assisted Sacrocolpopexy Using Autologous Posterior Rectus Sheath Restore Vaginal Support: The RESTORE Study' on April 22.

Study Type: Interventional

Study Design: Purpose: Treatment Allocation: Non-randomised trial Masking: Open (masking not used) Type of endpoint: Efficacy

Primary Sponsor: Epworth HealthCare

Condition: Pelvic organ prolapse Pelvic organ prolapse Reproductive Health and Childbirth - Other reproductive health and childbirth disorders

Intervention: Robot-assisted sacrocolpopexy using posterior rectus sheath (PRS) a novel alternative autologous graft for the treatment of pelvic organ p...