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the Indications and Clinical Efficacy of Pelvic Organ Prolapse Surgery

Pelvic Organ Prolapse Clinical Trial

Official title:
The Clinical Efficacy of Pelvic Organ Prolapse Surgery

Clinical Trial Summary

One thousand patients with stage＞2 POP are recruited. The patients are all received surgeries,such as transvaginal synthetic mesh surgery, the sacral fixation, tissue repair surgery and colpocleisis. The patients with POP who have not undergone surgery are excluded. Postoperatively, the investigators investigate the indications and clinical efficacy of pelvic organ prolapse surgery.

Clinical Trial Description

Postoperatively, the investigators analyze the patients' subjective and objective recurrent rates. The investigators compare the quality of life by filling out the preoperative and postoperative scoring questionnaires (PISQ 12, PFDI-20, PFIQ-7).The electrical physiological changes will be focused on. The investigators also use Overactive Bladder Symptom Score(OABss) to assess the lower urinary tract symptoms. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02599311
Study type Interventional
Source Peking University People's Hospital
Contact Xiuli Sun, professor
Phone 861088324354
Email zzucaotingting@163.com
Status Recruiting
Phase Phase 3
Start date August 2015
Completion date October 2020
View Details
See also
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Completed NCT01320631 - Male Sexual Experience and Its Impact on Quality of Life Before and After Their Sexual Partners Undergo Polypropylene Mesh Augmented Pelvic Floor Reconstruction N/A
Completed NCT00581412 - Composite Graft Use in Abdominal Sacrocolpopexy Reduces Erosion Rates N/A