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Not yet recruiting NCT07347847

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

— Observational Emergency Department Patient

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: No intervention.
Who it may be relevant to
Registry conditions: Emergency Department Patient. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

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.

Interventions

  • Other No intervention
    no intervention

Primary outcome measures

  • Death rate [Time frame: 30 days]
Secondary outcome measures (3)
  • Duration of hospitalization [Time frame: 30 days]
  • length of stay in the emergency department [Time frame: 30 days]
  • Rate of Adverse events [Time frame: 30 days]

Eligibility criteria

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

France · 7 centers
  • CHU Angers — Angers
  • CH Le Mans — Le Mans
  • CHU Nantes — Nantes
  • CHU Poitiers — Poitiers
  • CHU Strasbourg — Strasbourg
  • CHU Toulouse — Toulouse
  • CHU Tours — Tours

Identifiers

NCT: NCT07347847 · 35RC25_30013

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗