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A Randomized Controlled Trial Evaluating Uterine Preservation During Laparoscopic Sacrocolpopexy for the Treatment of Pelvic Organ Prolapse

A Randomized Controlled Trial Evaluating Uterine Preservation During Laparoscopic Sacrocolpopexy for the Treatment of Pelvic Organ Prolapse

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090075
Enrollment
Unknown
Registered
2024-09-24
Start date
2024-09-24
Completion date
Unknown
Last updated
2024-09-30

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

Conditions

Pelvic organ prolapse

Interventions

Non Uterus preserving group:Laparoscopic hysterectomy with sacrocolpopexy
Uterus Preserving group:Laparoscopic sacrocolpopexy without hysterectomy

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) POP mainly featuring middle pelvic compartment defects (Grade III or above based on POP-Q); (2) Sexually active patients aged between 45 and 60; (3) Completed fertility; (4) Voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Have a history of prolapse-related surgery, pelvic floor reconstruction surgery, or hysterectomy; (2) Have severe medical comorbidities; coagulation dysfunction; (3) Have fertility requirements; (4) Are in an acute inflammatory phase; (5) Have vaginal ulcers; (6) Have severe pelvic adhesions; (7) Have cervical and endometrial pathologies that is not suitable for uterine preservation.

Design outcomes

Primary

MeasureTime frame
Objective recurrence rate;

Secondary

MeasureTime frame
mesh related complications;pelvic organ prolapse related symptoms;Sexual satisfaction;surgery related indicators;

Countries

China

Contacts

Public ContactXin Yang

Peking University People's hospital

xinyang_2003@sina.com+86 139 0131 8932

Outcome results

None listed

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