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Enhanced Recovery after Surgery Program in Laparoscopic Sacrocolpopexy: A Randomized Controlled Trial

Enhanced Recovery after Surgery Program in Laparoscopic Sacrocolpopexy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056662
Enrollment
Unknown
Registered
2022-02-10
Start date
2022-02-28
Completion date
Unknown
Last updated
2023-09-04

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

Conditions

Pelvic Organ Prolapse

Interventions

Experimental group:ERAS
Control group:Conventional protocol

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age = 75 years; 2. Severe pelvic organ prolapse, conservative treatment is ineffective, and laparoscopic sacrocolpopexy is planned; 3. ASA class I - II; 4. No contraindication of laparoscopic surgery; 5. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Complicated with malignant tumor; 2. Liver and kidney dysfunction, mental illness; 3. Contraindications of laparoscopic surgery; 4. NSAIDs are contraindicated.

Design outcomes

Secondary

MeasureTime frame
Postoperative complications;Postoperative pain score;Readmission rate within 30 days after operation;—

Primary

MeasureTime frame
Postoperative hospital stay;—

Countries

China

Contacts

Public ContactLan Zhu

Peking Union Medical College Hospital

Zhu_julie@pumch.cn+86 13911714696

Outcome results

None listed

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