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Clinical Trial 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.


Clinical Trial Description

This observational prospective multicenter study will be conducted using data from electronic medical records, acquired as part of usual care, in patients admitted for acute dyspnea in the emergency department. Clinical, treatment, laboratory and imaging data acquired during the hospitalization (in the emergency department and in the department that admitted the patients following the emergency department stay) will be collected.

Vital status will be recorded at 30 days and 1 year post-admission. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03194243
Study type Observational
Source Central Hospital, Nancy, France
Contact Tahar CHOUIHED, MD
Phone + 33 3 83 85 14 96
Email t.chouihed@chru-nancy.fr
Status Recruiting
Phase N/A
Start date October 5, 2017
Completion date October 2023

See also
  Status Clinical Trial Phase
Not yet recruiting NCT02531542 - Evaluation of Rapid Emergency Echography for Acute Dyspnoea N/A
Recruiting NCT04240067 - Multimarker Approach for Acute Dyspnea in Elderly Patients Admitted in the Emergency Department
Recruiting NCT04817488 - Live Stream of Prehospital Emergency Ultrasound in Patients With Acute Dyspnoea