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Incidence and Severity of Acute Respiratory Distress Syndrome (ARDS) in the French Wounded Soldiers — SDRA-OPEX  

Acute Respiratory Distress Syndrome Clinical Trial

Official title:
Incidence and Severity of Acute Respiratory Distress Syndrome (ARDS) in the French Wounded Soldiers

Clinical Trial Summary

The purpose of this study is to evaluate the incidence of the ARDS in the French wounded soldiers.

Clinical Trial Description

The Acute Respiratory Distress Syndrome (ARDS) complicates war wounds. Among the repatriated wounded persons, it can appear in the first 7 days.

It has been well described among American soldiers and it is known that it's serious, frequent and multifactorial.

However, not a single study has described the frequency and the severity of the ARDS in French wounded soldiers.

Thus the purpose of this study is to estimate the incidence and severity of the ARDS among the French wounded soldiers, admitted in continuing care and intensive care unit between 2001 and 2017.

The analysis of this data collection will let us improve the medical care of the ARDS in Outside Operation. ;

Study Design

Related Conditions & MeSH terms

  • Acute Lung Injury
  • Acute Respiratory Distress Syndrome
  • Respiratory Distress Syndrome, Adult
  • Respiratory Distress Syndrome, Newborn
  • Syndrome
Clinical Trial Details
NCT number NCT03662230
Study type Observational
Source Direction Centrale du Service de Santé des Armées
Contact
Status Completed
Phase
Start date June 1, 2018
Completion date November 7, 2019
View Details
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