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Clinical Trials in France / NCT06235008
Starting soon Observational

PAthwAy of Dyspneic patIent in Emergency in the North-east Region (North-East PArADIsE)

NCT06235008 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2024-03-31
Last updated
2024-01-31

Condition(s) studied

Dyspnea

Study summary

This is an observational retrospective multi-center study in patients managed for acute dyspnea by Emergency department medical team.

The main aim of the study is to evaluate factors associated with mortality risks in patients managed for acute dyspnea by an Emergency department medical team, overall, as well as in subgroups of interest (male/female, age categories, mode of admission and comorbidities).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Man or women ≥ 18 years * Patients with acute dyspnea cared by a medical team of the emergencies of CHRU of Nancy, CHR Metz-Thionville and CH d'Epinal. Exclusion Criteria: * Cardiorespiratory arrest before medical management by the Emergency Department team * Adults under legal protection

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
CHRU Nancy France

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06235008 on ClinicalTrials.gov ↗ ← All trials in France