Stepped implementation of Enhanced Recovery After Surgery in major gynaecological surgery

A cluster randomised controlled trial of a stepped implementation strategy that aims at the normalisation of the Enhanced Recovery After Surgery programme in major gynaecological surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON22049

Enrollment

Registered

2013-07-02

Start date

2013-11-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

Perioperative care

Interventions

The intervention group receives an innovative stepped implementation strategy comprising four levels of intensity of support. Implementation starts with generic low-cost activities and builds up to th

Eligibility

Inclusion criteria

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

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.

Design outcomes

Primary

Measure	Time frame
The primary outcome is length of postoperative hospital stay.	—

Secondary

Measure	Time frame
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.	—

Contacts

Public ContactJ.J.A Groot, de

Postbus 616

jeanny.degroot@maastrichtuniversity.nl0031 (0)43 3882317

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)