Uterine prolapse, cystocele
Conditions
Interventions
Experimental group:Laparoscopic non-mesh cerclage pectopexy
Control group :Laparoscopic pectopexy
Sponsors
Department of Gynecology and Obstetrics, the University of Hong Kong - Shenzhen Hospital
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. cystocele POP-Q stage 2; 2. Patients has clinical manifestations of uterine and bladder prolapse, such as a sense of heaviness, back pain, dyspareunia, dysuria, and urinary incontinence; 3. Patients request surgical treatment.
Exclusion criteria
Exclusion criteria: 1. Women with previous pelvic floor or prolapse operation; 2. Acute pelvic infection; 3. Contraindications for laparoscopic operation (e.g. risk of severe adhesions); 4. Known malignancy of the cervix or cervical intraepithelial neoplasia; 5. Patients with malignant neoplasms of the reproductive system; 6. Pregnant women; 7. Patients have wishs to preserve fertility; 8. The patient has contraindications to surgery, such as serious diseases in internal medicine and are not suitable for surgery; 9. Language barriers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Success rate;Failure rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Complication rates;Operation time;Blood loss;Hospital stay;Visual analog scale of pain;PFDI-20;Prolapse quality of life questionnaire, P-QOL;Prolapse and incontinence sexual function questionnaire PISQ-IR;Patient gobal impression of improvement, PGI-I; | — |
Countries
China
Contacts
Public ContactWenju Zhang
The University of Hong Kong-Shenzhen Hospital
Outcome results
None listed