Recruiting soon

Fr-PArADIseFactors Influencing Mortality and Rehospitalization in Acute Dyspnea Emergencies

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Study Aim

This study aims to observe factors influencing mortality and rehospitalization in adults experiencing acute dyspnea emergencies after hospital discharge.

What is being collected

Data Collection

Collected from past medical records and data - Retrospective
Who is being recruted

Over 18 Years
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: September 2024
See protocol details

Summary

Principal SponsorPr. Nicolas GIRERD
Study ContactNicolas GIRERD, MD, PhDMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: September 30, 2024

Actual date on which the first participant was enrolled.

This observational retrospective multi-center study focuses on patients treated for acute dyspnea by emergency medical teams. The primary objective is to identify factors associated with the risk of mortality and rehospitalization in these patients. This evaluation will be conducted both overall and within specific subgroups of interest, including gender (men/women), age categories, mode of admission, and comorbidities.

Official TitlePAthwAy of Dyspneic patIent in Emergency in France
NCT06509854
Principal SponsorPr. Nicolas GIRERD
Study ContactNicolas GIRERD, MD, PhDMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

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

89700 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

Inclusion Criteria: * Man or women aged 18 years and older. * Patients with acute dyspnea managed by a medical emergency team at the investigator centers between 2010 and 2021. Exclusion Criteria: \- Cardiorespiratory arrest before emergency department management.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 4 locations

Suspended

CHU de Besançon

Besançon, FranceOpen CHU de Besançon in Google Maps
Suspended

CHU de Dijon

Dijon, France
Suspended

Hospices civils de Lyon, Groupement Hospitalier Édouard-Herriot

Lyon, France
Suspended

CHRU of Nancy

Nancy, France
Recruiting soon4 Study Centers