Actively Recruiting
Effectiveness of the RAUC Pathway in Reducing Unscheduled Hospitalizations After Emergency Digestive Surgery
Led by Centre Hospitalier Universitaire, Amiens · Updated on 2025-06-13
3000
Participants Needed
2
Research Sites
112 weeks
Total Duration
On this page
Sponsors
C
Centre Hospitalier Universitaire, Amiens
Lead Sponsor
U
University Hospital, Rouen
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Effectiveness of the RAUC Pathway in Reducing Unscheduled Hospitalizations After Emergency Digestive Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient consulted in emergency for a digestive pathology requiring surgery
- Adult patient (18 years old or older)
- Able to give consent
- Affiliated to a social security scheme
You will not qualify if you...
- 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
- Pregnant or breastfeeding woman
- Patient under guardianship, curatorship or deprived of liberty
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
CHU Rouen
Rouen, France, 76000
Actively Recruiting
2
Centre Hospitalier Universitaire, Amiens
Salouël, France, 80480
Actively Recruiting
Research Team
J
Jean Marc Regimbeau, Pr
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
3
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here