Pelvic organ prolapse
Conditions
Interventions
experimental group:transvaginal natural orifice transluminal laparoscopic high sacral ligament fixation
control group:traditional transvaginal uterosacral ligament suspension
Sponsors
The Third Affiliated Hospital of Guangzhou Medical University
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1.According to the POP Quantification system (POP-Q), patients who were confirmed that the uterine or vaginal top prolapse >= II degree, or the anterior vaginal wall prolapse >= II degree combined with the uterine or vagina top prolapse >= II degree, and has completed the childbirth; 2.Sexual life history; 3.Sign written consent form.
Exclusion criteria
Exclusion criteria: 1.History of rectal surgery, suspected rectovaginal septum endometriosis or tumor; 2.History of pelvic inflammatory disease; 3.Acute infection of the lower genital tract; 4.Pregnant.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| completion rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| visual analogue scale was used to evaluate pain at postoperative day 1 to 7;operation time;postoperative hospital stay;pelvic organ prolapse was scored by quantitative staging before surgery and at 6 weeks, 3 months and 1 year after surgery;intraoperative and postoperative complications 6 weeks, 3 months and 1 year;pelvic floor dysfunction questionnaire (PFIQ-7) and urinary incontinence questionnaire before and after surgery at 6 weeks, 3 months and 1 year;intraoperative blood loss; | — |
Countries
China
Contacts
Public ContactLin Qiongyan
The Third Affiliated Hospital of Guangzhou Medical University
Outcome results
None listed