A Long Term Prospective Observational Post Market Clinical Follow-Up (PMCF) Registry of Ethicon Gynecare Pelvic Mesh Products for The Treatment of Stress Urinary Incontinence and Pelvic Organ Prolapse
The objective of this post market, clinical registry is to evaluate the performance of the products of the TVT family of products or vaginal vault or uterine prolapse repair (with laparotomic or laparoscopic approach including robotic assisted) using either Gynemesh PS Mesh or Artisyn Mesh in women undergoing surgery for SUI and POP.
⁃ Patients who satisfy all of the following criteria will be considered eligible for enrollment in this registry:
⁃ SUI
• Stress urinary incontinence symptoms
• Urodynamic stress incontinence confirmed with urodynamic testing
• Female patient ≥ 21 years of age
• Desired surgical correction of SUI using synthetic pubo-urethral vaginal sling
• Planned surgery for primary SUI
• Patient able and willing to participate in follow-up
• Patient or authorized representative has signed the approved Informed consent POP
⁃ 1\. Uterine or vaginal vault prolapse symptoms 2. Urodynamic testing (optional) 3. Female patient ≥ 21 years of age 4. Desired surgical correction of POP using synthetic mesh 5. Planned surgery for uterine or vaginal vault prolapse with or without concomitant SUI surgery 6. Patient able and willing to participate in follow-up 7. Patient or authorized representative has signed the approved Informed consent