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Clinical Trials/NCT06769438
NCT06769438
Recruiting
Not Applicable

Effectiveness of the Augmented Rehabilitation of Digestive Surgical Emergencies Pathway in Reducing Unscheduled Hospitalizations After Surgery

Centre Hospitalier Universitaire, Amiens2 sites in 1 country3,000 target enrollmentJune 2, 2025

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Digestive Emergency
Sponsor
Centre Hospitalier Universitaire, Amiens
Enrollment
3000
Locations
2
Primary Endpoint
Occurrence of an unscheduled hospitalization readmission
Status
Recruiting
Last Updated
10 months ago

Overview

Brief Summary

The number of emergencies's visits (22 million visits in 2019 in France), the organization of emergencies and the sustainability of the current health system are threatened. In the CHUAP adult emergency department, 60,000 visits were recorded in 2022.

Unlike medical emergencies which have structured their care and research activities (heart, brain), and whose organization has demonstrated its general interest for society, digestive surgical emergencies, which involve complex patients (elderly people, comorbidities) , emergency situations and surgical procedures, have never been thought of globally in terms of personalized care and research pathways. Currently, patients treated in emergency are managed without a pre-established optimization program and without a dedicated pathway, where emergency constitutes a major risk factor for postoperative complications.

RAUCAMIENS evaluates a new care pathway implemented within the framework of the RHU RAUC : the implementation of the Enhanced rehabilitation after surgery (ERAS) and e-health devices for home monitoring, for patients treated in the emergency room for a digestive pathology. The purpose is to evaluate the effectiveness of the RAUC pathway in reducing the rate of unplanned hospitalization readmission after emergency digestive surgery 30 days postoperative.

Registry
clinicaltrials.gov
Start Date
June 2, 2025
End Date
August 2027
Last Updated
10 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Criterion linked to the protocol :
  • - Patient consulted in emergency for a digestive pathology requiring surgery
  • Search criteria:
  • Adult patient (≥ 18 years old),
  • Able to give consent,
  • Affiliation to a social security scheme

Exclusion Criteria

  • Criterion linked to the protocol:
  • Patient leaving hospitalization to a convalescent center
  • Patient requiring direct operating room (vital emergency or surgical revision)
  • Patient presenting to the emergency room for a postoperative complication
  • Patient directly admitted to intensive care
  • Search criteria:
  • Pregnant or breastfeeding woman
  • Patient under guardianship, curatorship or deprived of liberty

Outcomes

Primary Outcomes

Occurrence of an unscheduled hospitalization readmission

Time Frame: 30 days

Occurrence of an unscheduled hospitalization readmission following digestive surgery performed urgently within 30 days

Secondary Outcomes

  • incremental cost-utility ratio(30 days)
  • Clavien-Dindo score(30 days)
  • Duration of hospitalization linked to the first admission to perform emergency digestive surgery(30 days)
  • Quality of life score(0 day)
  • Quality of Life score(30 days)
  • STAI-Y scale(0 day)
  • Transition to emergency without hospitalization(30 days)
  • incremental cost-effectiveness ratio(30 days)

Study Sites (2)

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