Skip to content

The ARRC III Trial of Advanced Recovery Room Care (ARRC).

The ARRC III Trial of Advanced Recovery Room Care (ARRC).

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05836285
Acronym
ARRCIII
Enrollment
3000
Registered
2023-05-01
Start date
2023-04-18
Completion date
2025-12-31
Last updated
2024-08-14

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

Conditions

Economic Problems, Post-Surgical Complication

Keywords

postoperative complications, safety, health economics, quality of recovery after surgery, surgery, anaesthesia

Brief summary

A postoperative high-acuity model of care (ARRC) has been shown, in a prospective cohort study of approximately 850 patients, to produce a marked improvement in patient and hospital outcomes, and hospital costs, in medium risk patients (Ludbrook G et al., JAMA Surgery 2023). The goal of this observational study is to examine the outcomes after non-cardiac surgery of a larger group of medium risk patients receiving different forms of care -ARRC and usual ward care. The main questions it aims to answer are: what are the outcomes for patients and hospital after the different forms of care, who receives benefit from high acuity care, what underlies the improved outcomes seen with high acuity care.

Detailed description

Demand for essential surgery is growing, yet we face an increasingly complex casemix and budget challenges. New paradigms to deliver high value care are essential. Advanced Recovery Room Care (ARRC) is a model of care which, at RAH, has been shown to provide substantial improvements in patient outcomes, hospital utilisation, and costs of care. Specifically, it showed when compared to usual ward care: improved Days at Home after Surgery (primary outcome), decreased in-hospital complications, and decreased mortality at 1, 3 and 12 months. This model was cost-effective compared to usual ward care: ICER of approximately -$250 per DAH It is essential to collect high quality data on this model relevant to consumers and hospitals, in order to: * provide a robust mechanism to ensure outcomes are maintained, and ideally improved, within our institution * provide a mechanism to potentially allow benchmarking in the future, across institutions * better identify which surgical subgroups receive benefit from ARRC * provide a resource to generate and test hypotheses as to how these benefits are achieved. To that end, the ARRC II study database is to be refined to function in essence as an ongoing registry. This will be initially piloted at RAH, the subject of this study.

Interventions

OTHERARRC

Eligible for ARRC and managed in ARRC unit

OTHERUsual Care

Eligible for ARRC but managed elsewhere as no ARRC bed available

Sponsors

Royal Adelaide Hospital
CollaboratorOTHER
University of Adelaide
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Scheduled for elective or unplanned surgery * Scheduled to stay in hospital at least one night after surgery * 30-day mortality of 0.5% to 8% by the US National Safety and Quality Improvement Program risk score (NSQIP)

Exclusion criteria

* Undergoing cardiac surgery * Scheduled for postoperative Intensive Care Unit management

Design outcomes

Primary

MeasureTime frameDescription
Days at Home after surgery90 days after surgerynumber of days spent at usual place of residence within 90 days after surgery

Secondary

MeasureTime frameDescription
in-hospital complicationsout to 10 days after surgerymedical emergency response level complications
mortality12 months after surgerymortality out to 1 year after surgery
cost-effectiveness90 days after surgerycost per Day at Home improvement compared to usual care - Incremental cost-effectiveness ratio

Countries

Australia

Contacts

Primary ContactGuy L Ludbrook, MBBS PhD
guy.ludbrook@sa.gov.au+61 413817901
Backup ContactKathy Heyman, RN
kathy.heyman2@sa.gov.au+61 8 7074 5044

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026