Abdominal Sacral Colpopexy Using PVDF Mesh in Treatment of Uterovaginal Prolapse

Abdominal Sacral Colpopexy Using PVDF Mesh in Treatment of Uterovaginal Prolapse: A Mid-Term Review of Anatomical and Subjective Outcomes in Women with Vaginal Prolapse

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

TCTR

Registry ID

TCTR20220324006

Enrollment

Registered

2022-03-24

Start date

2015-04-01

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvic organ prolapse Pelvic Organ Prolapse

Interventions

Abdominal colpopexy surgery with mesh repair.In the beginning, we enter the peritoneum by creating a lower midline incision and then the anterior peritoneum. The intestines and colon are displaced to

Experimental Device

Abdominal Sacral Colpopexy Using PVDF Mesh

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Stage 3 or 4 pelvic organ prolapse, 2. Patients who have agreed to surgery with PVDF mesh

Exclusion criteria

Exclusion criteria: 1. history of pelvic radiation, 2. surgeries related to pelvic malignancies, 3. kidney transplantation

Design outcomes

Primary

Measure	Time frame
vaginal prolapse at 12 months after end of the surgery Pelvic Organ Prolapse Quantification (POP-Q) System	—

Secondary

Measure	Time frame
mesh erosion at any time after the surgery physical examination,sexual symptoms at 12 months after the surgery International Consultation on Incontinence Questionnaire Vaginal Symptoms Module (ICIQ-VS),vaginal symptoms at 12 months after the surgery International Consultation on Incontinence Questionnaire Vaginal Symptoms Module (ICIQ-VS)	—

Countries

Iran

Contacts

Public ContactMehdi Dehghani

Isfahan University of Medical Sciences

alzahra@mui.ac.ir36202087

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026