Stepped implementation of Enhanced Recovery After Surgery in major gynaecological surgery

• Conditions: Perioperative care; elective abdominal surgery, gynaecological oncologyPerioperatieve zorg, electieve abdominale chirurgie, gynaecologische oncologie

• Registration Number: NL-OMON22049
• Lead Sponsor: Maastricht University Medical Center (MUMC+)

Brief Summary

/A

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 14

Inclusion Criteria

All Dutch hospitals that are authorised in 2013 to perform major abdominal surgery in gynaecologic oncology patients are eligible for inclusion.

Exclusion Criteria

The hospitals that are already participating in a structured and documented local perioperative improvement programme will be excluded from this study to avoid interference between programmes.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcome is length of postoperative hospital stay.

Secondary Outcome Measures

Name	Time	Method
Additional outcome measures will be length of recovery, guideline adherence and implementation costs. An effect, economic, and process evaluation will be conducted throughout the trial.