Pelvic organ prolapse
Conditions
Interventions
Test group:Transvaginal Natural Orifice Endoscopic Presacral–Uterosacral Ligament Compound Suspension
Sponsors
Obstetrics and Gynecology Hospital of Fudan University
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Patients who have completed childbirth and have no further desire for fertility. 2. Patients who refuse conservative treatment or for whom conservative treatment has failed. 3. Patients who are willing to undergo surgery and are undergoing pelvic organ prolapse surgery for the first time. 4. Patients with stage II or higher uterine prolapse based on POP-Q scoring, primarily with middle compartment prolapse within the hymenal ring, and possibly with other site prolapses. 5. Patients may have concurrent urinary incontinence. 6. Patients who are willing to comply with regular follow-up after surgery.
Exclusion criteria
Exclusion criteria: 1. Patients with a subjective desire to reject this surgical procedure. 2. Patients with a history of previous pelvic prolapse surgery. 3. Patients with a history of uterine hysterectomy. 4. Patients with a strong desire to preserve the uterus. 5. Patients with severe medical or surgical conditions, tumors, infections, or bleeding disorders that make them unsuitable for surgery. 6. Patients suspected of or diagnosed with malignant pelvic tumors.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Surgical success outcomes; | — |
Secondary
| Measure | Time frame |
|---|---|
| Primary perioperative evaluation indicators;Functional outcomes;postoperative complications; | — |
Countries
China
Contacts
Public ContactYisong Chen
Obstetrics and Gynecology Hospital of Fudan University
Outcome results
None listed