SmartCPR Trial: An Analysis of a Waveform-Based Automated External Defibrillation (AED) Algorithm on Survival From Out-of-Hospital Ventricular Fibrillation

NCT00535106 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 900

Last updated 2009-10-19

No results posted yet for this study

Summary

This study is designed to examine the impact of an available technology within an automated external defibrillator (AEDs) to improve survival following out-of-hospital cardiac arrest for patients presenting in ventricular fibrillation.

Conditions

  • Ventricular Fibrillation
  • Cardiac Arrest

Interventions

DEVICE

Automated external defibrillator (Philips FR2+ AED)

Patients in this arm will be provided with immediate defibrillatory shock coupled with otherwise standard resuscitative efforts.

DEVICE

SmartCPR

Patient in this arm will be treated with standard resuscitation efforts except that the first AED analysis will utilize an waveform-based algorithm to recommend either immediate defibrillation or delayed defibrillation for each patient.

OTHER

Delayed defibrillation

In New York City only, all patients not initially treated by study personnel will receive other regional standard for resuscitation - delayed defibrillation.

Sponsors & Collaborators

  • Philips Medical Systems

    collaborator INDUSTRY
  • London Ambulance Service

    collaborator OTHER
  • New York City Fire Department

    lead OTHER_GOV

Principal Investigators

  • John P Freese, MD · New York City Fire Department

  • Bradley J Kaufman, MD, MPH · New York City Fire Department

  • Rachael Donohoe, PhD · London Ambulance Service

  • Dawn Jorgenson, PhD · Philips Medical Systems

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-05-31
Primary Completion
2009-06-30
Completion
2009-06-30

Countries

  • United States
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00535106 on ClinicalTrials.gov