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Not yet recruitingNCT06509854Fr-PArADIseUpdated Jul 22, 2024

PAthwAy of Dyspneic patIent in Emergency in France

An observational study in Acute Dyspnea, sponsored by Pr. Nicolas GIRERD. Not yet recruiting at 4 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-07-22.

Sponsored by Pr. Nicolas GIRERD · Observational

From the registry’s dates

  • Primary completion was expected by Sep 2025, 1 year ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
89,700
Ages
18 Years and older
Sex
All
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Study 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.

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Conditions studied

  • Acute Dyspnea

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03

In context

Dyspnea

656 studies on the registry are indexed under Dyspnea; 153 are open to participants now.

This study's planned enrollment of 89,700 is above the median of 122 across 204 observational studies indexed under Dyspnea.

Browse Dyspnea studies →

Lead sponsor

Pr. Nicolas GIRERD is the lead sponsor of 10 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult patients treated in the emergency department for acute dyspnea.

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

Exclusion Criteria:

  • Cardiorespiratory arrest before emergency department management.
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
89,700 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. All-cause post-hospitalization mortality and rehospitalization

    Composite endpoint of all-cause post-hospitalization mortality and rehospitalization

    Time frame: Within 5 years following hospital discharge

Secondary outcomes

  1. Proportion of readmissions (all-cause and specific - including hospitalization for acute dyspnea ).

    Time frame: 1 month and 1 year post admission for acute dyspnea in the emergency department

  2. Post admission mortality

    Assessed by: Composite criterion of rehospitalization and/or death following emergency department admission (short and long-term). with outcome 5.

    Time frame: Within 20 years following hospital discharge

  3. Post admission rehospitalization

    Assessed by: Composite criterion of rehospitalization and/or death following emergency department admission (short and long-term) with outcome with outcome 4.

    Time frame: Within 20 years following hospital discharge

  4. Erroneous etiological diagnosis of dyspnea in the emergency department

    Assessed by: defined as a discrepancy between the diagnosis at discharge from the emergency department and the final diagnosis in the hospital discharge letter

    Time frame: Within hospital stay, maximum 21 days

  5. All-cause mortality and specific mortality (cardiovascular and non-cardiovascular).

    Assessed by: Composite endpoint of all-cause mortality and specific mortality (cardiovascular and non-cardiovascular) with outcome 8

    Time frame: Within 5 years following hospital discharge

  6. Emergency post-admission mortality

    Assessed by: Composite criterion of mortality and rehospitalization post-admission for acute dyspnea in the emergency department over the long term with outcome 9

    Time frame: Within 20 years following hospital discharge

  7. Emergency post-admission rehospitalisation

    Assessed by: Composite criterion of mortality and rehospitalization post-admission for acute dyspnea in the emergency department over the long term outcome 8

    Time frame: Within 20 years following hospital discharge

  8. Duration of stay in the emergency department

    Assessed by: Duration of stay in the emergency department

    Time frame: Within hospital stay, maximum 21 days

  9. Erroneous etiological diagnosis of dyspnea in the emergency department

    Assessed by: Erroneous etiological diagnosis of dyspnea in the emergency department

    Time frame: Within hospital stay, maximum 21 days

  10. In-hospital mortality

    Assessed by: In-hospital mortality

    Time frame: Within hospital stay, maximum 21 days

  11. Length of hospital stay

    Assessed by: Length of hospital stay

    Time frame: Within hospital stay, maximum 21 days

  12. Post emergency admission (For dyspnea) mortality and rehospitalization

    Assessed by: Post emergency admission (For dyspnea) mortality and rehospitalization

    Time frame: Within 5 years following hospital discharge

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Study locations

4 sites
  • CHU de Besançon
    Besançon, France
    • Omide TAHERI · Contact
    • Omide TAHERI, MD · Principal investigator
    • Johan COSSUS, MD · Principal investigator
  • CHU de Dijon
    Dijon, France
    • Patrick RAY, MD, PhD · Contact
    • Patrick RAY, MD, PhD · Principal investigator
  • Hospices civils de Lyon, Groupement Hospitalier Édouard-Herriot
    Lyon, France
    • Stephanie BOSNE, MD · Contact
    • Stéphanie BOSNE, MD · Principal investigator
    • Karim TAZAROURTE, MD, PhD · Principal investigator
  • CHRU of Nancy
    Nancy, France
    • Tahar CHOUIHED · Contact · t.chouihed@chru-nancy.fr · +33383157322
    • Nicolas GIRERD · Contact · n.girerd@chru-nancy.fr · 0383157322
    • Tahar CHOUIHED, MD, PhD · Principal investigator
    • Nicolas GIRERD, MD, PhD · Principal investigator
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 22, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06509854
Lead sponsor
Pr. Nicolas GIRERD
Responsible party
Pr. Nicolas GIRERD (Clinical Professor, Central Hospital, Nancy, France) — Sponsor-investigator
First posted
Jul 19, 2024
Start date
Sep 30, 2024 (estimated)
Primary completion
Sep 30, 2025 (estimated)
Completion
Sep 30, 2031 (estimated)
Last update
Jul 22, 2024

Study contacts

Nicolas GIRERD, MD, PhD
Contact
n.girerd@chru-nancy.fr
+33383157322
Tahar CHOUIHED, MD, PhD
Contact
t.chouihed@chru-nancy.fr
+33383157322
Tahar CHOUIHED, MD, PhD
principal investigator · Central Hospital, Nancy, France
Nicolas GIRERD, MD, PhD
principal investigator · CHRU de Nancy

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2024. You cannot join it, but the record below documents what was studied.

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