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...