Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
970

Summary

Conditions
Out of Hospital Cardiac Arrest
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

The design consists in a multicenter national randomized open parallel group trial. All eligible patients with SCD will be included and randomized by the Emergency Medical Service (EMS) to one of the 2 following arms: immediate CA vs delayed CA. Patients randomized in the immediate CA group will be ...

The design consists in a multicenter national randomized open parallel group trial. All eligible patients with SCD will be included and randomized by the Emergency Medical Service (EMS) to one of the 2 following arms: immediate CA vs delayed CA. Patients randomized in the immediate CA group will be admitted directly to the catheterization laboratory. Patients randomized in the delayed CA will be admitted to the intensive care unit and a CA will be planned 48 to 96 hours after admission. Investigators can perform the CA in the delayed group < 48 hours if the following events appear: ST segment elevation or new left bundle branch block on the ECG Shock unresponsive to inotropes "Electrical storm" (repeated Ventricular Tachycardia (VT)/Ventricular Fibrillation (VF)) Segmental hypokinesia or akinesia on an echocardiogram Echocardiography and assessment of neurological status are done at discharge form the Intensive Care Unit, at hospital discharge and during the follow-up visits (90 and 180 days).

Tracking Information

NCT #
NCT02876458
Collaborators
Ministry of Health, France
Investigators
Principal Investigator: Christian Spaulding, MD, PhD Assistance Publique - Hôpitaux de Paris