Impact on Mortality of Hospitalisation of a Patient in a Hospital Bed That Does Not Correspond to His Needs After a Visit to the Emergency Department (RIGHT BED)

January 16, 2026 updated by: Rennes University Hospital

The aim of this study is to assess the impact of hospitalisation outside the referral requested by the emergency doctor on the mortality of patients admitted to emergency departments.

Study Overview

Status

Not yet recruiting

Conditions

Emergency Department Patient

Intervention / Treatment

Other: No intervention

Study Type

Observational

Enrollment (Estimated)

2766

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Name: François Saget, Md
Phone Number: +33299284321
Email: francois.saget@chu-rennes.fr

Study Locations

France
- - Angers, France
    - CHU Angers
    - Principal Investigator:
      
      Delphine Douillet
    - Contact:
      
      Delphine DOUILLET
      
      Phone Number: +33241353637
      
      Email: delphine.douillet@chu-angers.fr
  - Le Mans, France
    - CH Le Mans
    - Contact:
      
      Lionel Imsaad
      
      Phone Number: +332 43 43 43 43
      
      Email: limsaad@ch-lemans.fr
    - Principal Investigator:
      
      Lionel Imsaad
  - Nantes, France
    - CHU Nantes
    - Principal Investigator:
      
      Emmanuel Montassier
    - Contact:
      
      Emmanuel Montassier
      
      Phone Number: +332 40 08 33 33
      
      Email: Emmanuel.MONTASSIER@chu-nantes.fr
  - Poitiers, France
    - CHU Poitiers
    - Principal Investigator:
      
      Nicolas MARJANOVIC
    - Contact:
      
      Nicolas Marjanovic
      
      Phone Number: +330549444444
      
      Email: nicolas.marjanovic@chu-poitiers.fr
  - Strasbourg, France
    - CHU Strasbourg
    - Contact:
      
      Pierrick Le Borgne
      
      Phone Number: +333 88 11 67 68
      
      Email: pierrick_med@yahoo.fr
    - Principal Investigator:
      
      Pierrick Le Borgne
  - Toulouse, France
    - Chu Toulouse
    - Contact:
      
      Margaux Piechowiak
      
      Phone Number: +335 61 77 22 33
      
      Email: Piechowiak.m@chu-toulouse.fr
    - Principal Investigator:
      
      Margaux Piechowiak
  - Tours, France
    - CHU Tours
    - Contact:
      
      Geoffroy Rousseau
      
      Phone Number: +332.47.47.47.47
      
      Email: geoffroy.rousseau@chu-tours.fr
    - Principal Investigator:
      
      Geoffroy Rousseau

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

Adult
Older Adult

Accepts Healthy Volunteers

Sampling Method

Non-Probability Sample

Study Population

- People Presenting at an emergency department

Description

Inclusion Criteria:

Presenting at an emergency department participating in the study,
Requiring hospitalisation

Exclusion Criteria:

Patients hospitalised in short-stay units with secondary outpatient care,
Adults subject to legal protection (legal guardianship, curatorship, trusteeship), persons deprived of their liberty.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Death rate Time Frame: 30 days	30 days

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Duration of hospitalization Time Frame: 30 days		30 days
length of stay in the emergency department Time Frame: 30 days		30 days
Rate of Adverse events Time Frame: 30 days	Adverse events occuring during hospitalization	30 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Rennes University Hospital

Investigators

Study Chair: François Saget, francois.saget@chu-rennes.fr

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

January 1, 2026

Primary Completion (Estimated)

September 1, 2026

Study Completion (Estimated)