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Clinical Trial Summary

The goal of this study is to show the superiority in survival at hospital admittance and in neurological outcome on hospital discharge of continuous mechanical chest compression using LUCAS device versus manual chest compressions in patients who suffered an out-of-hospital cardiac arrest.


Clinical Trial Description

The primary goals of the trial are:

- To show a survival increase at hospital admittance after out-of-hospital cardiac arrest of patients treated by continuous chest compressions LUCAS device compared with patients treated by manual chest compressions.

- To evaluate neurological outcome on hospital discharge, in two centres (Vall d'Hebron Hospital and Josep Trueta Hospital). ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01521208
Study type Interventional
Source Sistema d’Emergències Mèdiques
Contact Francesc Carmona Jiménez, Doctor
Phone +34607847717
Email franciscojosecarmona@gencat.cat
Status Recruiting
Phase Phase 3
Start date January 2012
Completion date April 2014

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