NCT03194243

Brief Summary

This is an observational prospective multicenter study of patients admitted for acute dyspnea in an emergency department of the participating centers in the Lorraine district. The primary objective is to assess the outcome of this population according to the cause of acute dyspnea as well as identify the predictors of this outcome, both overall and according to each acute dyspnea cause.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
75,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2017

Longer than P75 for all trials

Geographic Reach
1 country

9 active sites

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 29, 2017

Completed
23 days until next milestone

First Posted

Study publicly available on registry

June 21, 2017

Completed
4 months until next milestone

Study Start

First participant enrolled

October 5, 2017

Completed
6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2023

Completed
Last Updated

October 10, 2017

Status Verified

October 1, 2017

Enrollment Period

6 years

First QC Date

May 29, 2017

Last Update Submit

October 9, 2017

Conditions

Acute Dyspnea

Keywords

acute dyspneaacute heart failureemergency

Outcome Measures

Primary Outcomes (1)

  • All cause mortality

    From emergency admission for acute dyspnea up until 1 year

Secondary Outcomes (21)

  • Demographic data

    through hospital stay, an average of 10 days

  • Clinical data

    through hospital stay, an average of 10 days

  • Treatment data

    through hospital stay, an average of 10 days

  • Laboratory data

    through hospital stay, an average of 10 days

  • Imaging data

    through hospital stay, an average of 10 days

  • +16 more secondary outcomes

Study Arms (1)

Patients admitted for acute dyspnea

Patients admitted for acute dyspnea in the emergency department

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with acute dyspnea and treated in an emergency department of the participating centers in the Lorraine district.

You may qualify if:

  • Men or women \> or = 18 years.
  • Patients with acute dyspnea admitted for acute dyspnea in the emergency department.
  • Patient informed.

You may not qualify if:

  • Cardiorespiratory arrest.
  • Patient having expressed his or her opposition.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (9)

CH EPINAL - Service des Urgences

Épinal, Lorraine, 88021, France

RECRUITING

CH Marie-Madeleine FORBACH - Service des Urgences

Forbach, Lorraine, 57604, France

RECRUITING

CH LUNEVILLE - Service des Urgences

Lunéville, Lorraine, 54 301, France

RECRUITING

CHR METZ-THIONVILLE- Hôpital de Mercy- Service des Urgences

Metz, Lorraine, 57085, France

RECRUITING

CHRU Nancy - Service des Urgences

Nancy, Lorraine, 54000, France

RECRUITING

CH PONT A MOUSSON- Service des Urgences

Pont-à-Mousson, Lorraine, 54 701, France

RECRUITING

CH REMIREMONT - Service des Urgences

Remiremont, Lorraine, 88204, France

RECRUITING

CH SAINT-DIE-DES-VOSGES - Service des Urgences

Saint-Dié, Lorraine, 88100, France

RECRUITING

CHR METZ-THIONVILLE- Hôpital Bel-Air- Service des Urgences

Thionville, Lorraine, 57100, France

RECRUITING

Related Publications (1)

  • Buessler A, Chouihed T, Duarte K, Bassand A, Huot-Marchand M, Gottwalles Y, Penine A, Andre E, Nace L, Jaeger D, Kobayashi M, Coiro S, Rossignol P, Girerd N. Accuracy of Several Lung Ultrasound Methods for the Diagnosis of Acute Heart Failure in the ED: A Multicenter Prospective Study. Chest. 2020 Jan;157(1):99-110. doi: 10.1016/j.chest.2019.07.017. Epub 2019 Aug 2.

    PMID: 31381880DERIVED

MeSH Terms

Conditions

Emergencies

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Tahar CHOUIHED, MD

    Central Hospital, Nancy, France

    PRINCIPAL INVESTIGATOR

  • Nicolas GIRERD, MD,PhD

    Central Hospital, Nancy, France

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Tahar CHOUIHED, MD

CONTACT

+ 33 3 83 85 14 96t.chouihed@chru-nancy.fr

Nicolas GIRERD, MD,PhD

CONTACT

+ 33 3 83 15 74 96n.girerd@chru-nancy.fr

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 29, 2017

First Posted

June 21, 2017

Study Start

October 5, 2017

Primary Completion

October 1, 2023

Study Completion

October 1, 2023

Last Updated

October 10, 2017

Record last verified: 2017-10

Data Sharing

IPD Sharing
Will not share

Locations

FR(9)