Pelvic organ prolapse
Conditions
Interventions
Experimental group:Transvaginal Uterus Sling
Sponsors
Department of Urology, West China Hospital, Sichuan University
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Patients with pelvic organ prolapse stage >= II according to POP-Q score and who are willing to undergo surgery; 2. Postmenopausal patients; 3. Patients with complete uterine atrophy.
Exclusion criteria
Exclusion criteria: 1. Patients with a history of total or partial hysterectomy; 2. Patients with a history of total or partial hysterectomy of the cervix; 3. Patients with uterus-related diseases (e.g. fibroids, abnormal uterine bleeding, etc.); 4. Patients with a history of cervical radiotherapy; 5. Patients with abnormal cervical cytology; 6. Patients with a history of lower abdominal and pelvic surgery; 7. Patients with coagulation disorders; 8. Patients with severe concomitant diseases that cannot tolerate surgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pelvic Organ Prolapse Quantification (POP-Q) System;Pelvic Floor Distress Inventory (PFDI-20);Complications; | — |
Countries
China
Contacts
Public ContactHong Shen
Department of Urology, West China Hospital, Sichuan University
Outcome results
None listed