PAthwAy of Dyspneic patIent in Emergency in France
Fr-PArADIse
1 other identifier
observational
89,700
1 country
4
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2024
Longer than P75 for all trials
4 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 4, 2024
CompletedFirst Posted
Study publicly available on registry
July 19, 2024
CompletedStudy Start
First participant enrolled
September 30, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2031
ExpectedJuly 22, 2024
July 1, 2024
1 year
July 4, 2024
July 18, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
All-cause post-hospitalization mortality and rehospitalization
Composite endpoint of all-cause post-hospitalization mortality and rehospitalization
Within 5 years following hospital discharge
Secondary Outcomes (12)
Proportion of readmissions (all-cause and specific - including hospitalization for acute dyspnea ).
1 month and 1 year post admission for acute dyspnea in the emergency department
Post admission mortality
Within 20 years following hospital discharge
Post admission rehospitalization
Within 20 years following hospital discharge
Erroneous etiological diagnosis of dyspnea in the emergency department
Within hospital stay, maximum 21 days
All-cause mortality and specific mortality (cardiovascular and non-cardiovascular).
Within 5 years following hospital discharge
- +7 more secondary outcomes
Eligibility Criteria
Adult patients treated in the emergency department for acute dyspnea.
You may qualify if:
- 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.
You may not qualify if:
- \- Cardiorespiratory arrest before emergency department management.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (4)
CHU de Besançon
Besançon, France
CHU de Dijon
Dijon, France
Hospices civils de Lyon, Groupement Hospitalier Édouard-Herriot
Lyon, France
CHRU of Nancy
Nancy, France
Study Officials
- PRINCIPAL INVESTIGATOR
Tahar CHOUIHED, MD, PhD
Central Hospital, Nancy, France
- PRINCIPAL INVESTIGATOR
Nicolas GIRERD, MD, PhD
CHRU de Nancy
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Clinical Professor
Study Record Dates
First Submitted
July 4, 2024
First Posted
July 19, 2024
Study Start
September 30, 2024
Primary Completion
September 30, 2025
Study Completion (Estimated)
September 30, 2031
Last Updated
July 22, 2024
Record last verified: 2024-07