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A prospective randomized study comparing improvement pelvic floor reconstruction and laparoscopic sacral fixation in the treatment of pelvic organ prolapse

A prospective randomized study comparing improvement pelvic floor reconstruction and laparoscopic sacral fixation in the treatment of pelvic organ prolapse

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15006044
Enrollment
Unknown
Registered
2015-03-06
Start date
2015-07-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvic organ prolapse

Interventions

One:improvement pelvic floor reconstruction
Two: laparoscopic sacral fixation

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. To be aged 55 to 65 years old woman, suffering from the symptoms of prolapse or vault prolapse POP-Q III-IV stage, suitable for surgery, the researchers agreed to participate and signed informed consent; 2. The combined stress incontinence need simultaneously transvaginal mid urethral sling (TVT-O).

Exclusion criteria

Exclusion criteria: Generally poor, difficult to tolerate serious medical complications of laparoscopic surgery; 1. A history of pelvic organ prolapse surgery patch application; 2. Reproductive system, urinary system, or with active systemic infection, surgery can be postponed until after the infection cleared; 3. Coagulation disorders or are receiving therapeutic anticoagulation drugs; 4. Who had previously received chemotherapy or pelvic radiation therapy; 5. Affects bladder or bowel function systemic diseases (such as Parkinson's disease, multiple sclerosis, spina bifida, spinal cord injury, etc.); 6. Patients with chronic pelvic pain; 7. Poorly controlled chronic cough; 8. BMI=30; 9. The researchers believe there may be other medical or mental illness can not be with the completion of the investigator.

Design outcomes

Primary

MeasureTime frame
Rate of Complication;

Contacts

Public ContactZhu Lan
zhu_julie@vip.sina.com+86 13911714696

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026