Ventricular fibrillation/cardiac arrest Circulatory System Cardiac arrest
Conditions
Interventions
This will be a safety and feasibility study which aims to show equivalence in the removal of ventricular fibrillation during cardiac arrests between a novel low-tilt defibrillating device and the stan
Sponsors
Royal Hospitals Trust (UK)
Eligibility
Inclusion criteria
Inclusion criteria: All adult patients in cardiac arrest with ventricular fibrillation as the identified rhythm.
Exclusion criteria
Exclusion criteria: Patients with existing 'Do not resuscitate' orders.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint of the study will be termination of ventricular arrhythmia for greater than or equal to five seconds following shock delivery. This will be determined by analysis of the defibrillator Electrocardiogram (ECG) tracing post-cardiac arrest. | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcome measures | — |
Countries
United Kingdom
Outcome results
None listed