Skip to main content
OpenTrials
Completed

NCT Number: NCT00139542

AED Use in Out-of-Hospital Cardiac Arrest: A New Algorithm Named "One Shock Per Minute"

The aim of the trial is to evaluate a new AED algorithm that proposes a new timeline between the time devoted to administer a defibrillation shock, and the time devoted to chest compressions.

The researchers propose to decrease the periods of interruption of cardiopulmonary resuscitation (CPR), while keeping the principle of early defibrillation.

Completed

Looking for future studies?

Notify Me

Key information

Age range

1 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Fire Brigade of Paris Emergency medicine department

Paris, 75017, France

About this study

Early use of semi-automated external defibrillators (AED) by Emergency Care teams in out-of-hospital cardiac arrest (OHCA), has been correlated with a significant gain in sequelae-free survival. The AED is programmed with an algorithm based recommended guidelines.

We will test a new algorithm that takes into account recent findings in pathophysiology.

Patients presenting with cardiovascular and pulmonary arrest treated by the BSPP Emergency Care who meet inclusion criterion are proposed for inclusion in the trial.

The aim of the trial is to evaluate a new AED algorithm that proposes a new timeline between the time devoted to administer a defibrillation shock, and the time devoted to chest compressions.

The new algorithm is entitled "one shock per minute". Use of this algorithm should validate several hypotheses:

  • the importance of administering cardiac massage and artificial ventilation (CPR) prior to initiation of electrical shock treatment.
  • the importance of continuing CPR immediately following electrical shock treatment
  • the importance of reducing time between CPR procedures to a minimum
  • the fact that three successive electrical shocks are of no therapeutic benefit.

We want to compare the control algorithm with the new one titled "one shock per minute", for shocked patients.

The sample size of this trial was calculated to provide a power of 85% and a type 1 error rate of alpha = 0.0294 for detecting an 11% increase in the rate of hospital admission, from its historical rate of 34% to a new rate of 45%. One interim analysis was planned with the stopping boundary alpha = 0.0294. This required inclusion of 430 patients in each group.

The primary endpoint is defined as "the admission of the patient alive at the hospital".

The secondary endpoints are defined as following :

  • Detection of Palpable Carotid Pulse (ROSC) within the first 8 minutes after the connection of the AED The other secondary endpoint is survival to one year.

Concerning patients that do not receive shocks

They represent a priori 82% of the patients. The absolute number is a priori 3940, that is to say, 1970 in both two groups.

They will be used for an advanced observational descriptive study, to establish hypothesis for future studies.The same primary and secondary endpoints will be evaluated for them.

Among these patients not shocked, the algorithm foresees 60 seconds of CPR for the Control Group, and 90 seconds for the Trial Group. This setting relies on the hypothesis that increasing the time dedicated to chest compressions will increase the probability of return of a palpable pulse (ROSC), even for patients who do not fibrillate.

Statistical analysis will be completed by "Hôpital d'Instruction des Armées BEGIN - Epidemiology department"

We propose a comparison using the Chi square test for qualitative variables, Student's t test for quantitative variables, completion of a logistics model to analyze prognostic factors, as well as the proportional hazards model for survival analysis. Tests will be bilateral (significant p = 0,029 if we consider one intermediate analysis).

Overall analysis strategy will be defined and completed by the Epidemiology department of Hôpital d'Instruction des Armées BEGIN

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients in a state of apparent death as noted on arrival of the emergency care team vehicle
  • Resuscitation by first aid team with a minimum of three people
  • Analysis of cardiac rhythm by the AED possible
  • At least one appropriate shock delivered by the AED

Exclusion criteria

  • Many victims (>3) that must be treated simultaneously
  • Signs of certain death (lividity)
  • Patient with palpable pulse on arrival of emergency care team
  • Patient already connected to another device
  • Incident involving an AED that requires a "materiovigilance" report

Treatment and study plan

One shock per minute AED protocol

Other

Single shocks; No post-shock pulse checks; 60 sec CPR before first shock; 30 sec CPR between rhythm analysis and shock delivery.

Other names: Biphasic LIFEPAK(R) 500 AED with cprMAX technology

Guidelines 2000 AED protocol

Other

Up to 3 consecutive shocks in a stack; No initial CPR prior to the first shock; Post-shock pulse checks after each non-shockable rhythm analysis; 60 sec CPR after each non-shockable rhythm analysis.

Other names: Biphasic LIFEPAK(R) 500 AED with cprMAX technology

Primary outcomes

  1. the number of patients appropriately shocked by AED admitted alive at hospital / the total number of patients appropriately shocked by AED

    Time frame: within the first day after the first cardiac arrest

Secondary outcomes

  1. Concerning patients appropriately shocked by AED: - return of spontaneous circulation (ROSC) at the arrival of physician on the scene

    Time frame: within the first hour after the first cardiac arrest

  2. - ROSC within the first 8 minutes after the connection of the AED

    Time frame: within the 8 minutes after the connection of the AED

  3. - Patient survival determined throughout the followup period of 1 year post-arrest.

    Time frame: one year after cardiac arrest

  4. Safety endpoints were occurrences of CPR-related hemothorax requiring thoracic drain and/or hemorrhagic lesions requiring transfusion

    Time frame: within days of the cardiac arrest

  5. Concerning patients not shocked by AED: - ROSC within the first 8 minutes after the connection of the AED

    Time frame: day of the cardiac arrest

  6. - patient admitted alive to the hospital

    Time frame: within 24-48 hours of the cardiac arrest

Sponsors and collaborators

Lead sponsor

Fire Brigade Of Paris Emergency Medicine Dept

Other

Collaborators

  • Brigade de Sapeurs Pompiers de Paris
  • Physio-Control, Inc, A division of Medtronic

Registry information

Official study title

Automated External Defibrillator (AED) Use in Out-of-Hospital Cardiac Arrest: A New Algorithm Named "One Shock Per Minute"

Acronym: DEFI2005

Important dates

Study start
2005
Primary completion
2007
Study completion
2008
First posted
Aug 31, 2005
Registry last updated
May 11, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.