Autopsy report · NCT03004885

Enhanced Lung Protective Ventilation for ARDS Patients With PrismaLung

Cause of deathOther Automatic label, confidence 0.3, unverified. How labels are made.

“Insufficient CO2 removal obtained with the PrismaLung membrane oxygenator”

The sponsor’s own words in the registry.

Life of this trial

Registered 10 months before it started.
Ran for about 2 months before it stopped.
1 participant enrolled.
No results are posted on the registry.

Vital statistics

Status: Terminated
Phase: Na
Sponsor: Hôpital Européen Marseille
Sponsor type: University, hospital or other
Conditions: Acute Respiratory Distress Syndrome
Interventions: PrismaLung
Participants: 1
Sites: 1
Countries: France

Look deeper

The official registry record (the source of truth)
Record history: every change the sponsor made
Open it in the database

Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.