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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03662230
Acronym
SDRA-OPEX
Enrollment
100
Registered
2018-09-07
Start date
2018-06-01
Completion date
2019-11-07
Last updated
2020-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Respiratory Distress Syndrome

Keywords

war wounds, intensive care unit

Brief summary

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

Detailed 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.

Interventions

None listed

Sponsors

Direction Centrale du Service de Santé des Armées
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient evacuated from the theatre of outside operation and hospitalized in intensive care unit in France between 2001 et 2017

Exclusion criteria

* Opposition to the use of personal data

Design outcomes

Primary

MeasureTime frameDescription
Incidence of ARDSDay 7The appearance of ARDS is defined by a ratio of partial pressure arterial oxygen (PaO2) and fraction of inspired oxygen (FiO2) lower than 300 in 7 days after the wound.

Secondary

MeasureTime frameDescription
Assess the severity of ARDS7 daysthe severity of ARDS will be assessed regarding the necessity or not of non-invasive and invasive ventilation
Description of the severity of ARDS7 daysthe therapeutic intensity will be describe with : Maximal Positive end-expiration pressure (PEEP), curarisation, nitrogen monoxide (NO), prone position , Extracorporeal membrane oxygenation.
MortalityDay 90Assess the mortality since hospitalization
Assessment of the severity of ARDS7 daysthe severity of ARDS will be assessed regarding duration of non-invasive and invasive ventilation

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026