U.S., July 16 -- ClinicalTrials.gov registry received information related to the study (NCT07066761) titled 'Safety and Performance of a Pelvic Floor Mesh Implant (LatGYNious)' on July 04.
Brief Summary: The purpose of the clinical investigation is to verify that the investigational device (LatGYNious) is appropriate to significantly improve the pelvic organ prolapse in patients.
Study Start Date: July 01
Study Type: INTERVENTIONAL
Condition:
Pelvic Organ Prolapse (POP)
Genital Prolapse
Uterus Prolapse
Laparoscopic Surgery
Intervention:
DEVICE: Laparoscopic lateral suspension with surgical mesh (LatGYNious)
Laparoscopic lateral suspension with LatGYNious (with uterus preservation or after hysterectomy)
Recruitment Status: RECRUITIN...