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Clinical Trial Summary

The study is a prospective study at a single institution. Investigators create strict inclusion and exclusion criteria, selecting 124 patients with POP(≥II degree and have symptoms that need operation) . 62 patients in the intervention group accept extraperitoneal high uterosacral ligament suspension. The other 62 patients in the other group accept sacrospinous ligament suspension.


Clinical Trial Description

Investigators evaluate all women's operation method, operation time, bleed volume, overactive bladder questionnaire, PFDI-20,ICIQ-SF, I-QoL, PISQ-12, PFIQ-7, UDI-6, pre- and post-operation (at 1 month, 3 months, 6months and 1 year). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05189665
Study type Interventional
Source Peking University People's Hospital
Contact xiuli sun, professor
Phone 010-88324354
Email [email protected]
Status Recruiting
Phase N/A
Start date October 1, 2021
Completion date April 2023

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