AED 3 Post-Approval Study

N/AActive Not RecruitingNCT05013333

Zoll Medical Corporation38 enrolled

Overview

Demonstrate appropriate CPR sensor placement on pediatric and adult patients and demonstrate delivery of appropriate energy level of shocks to pediatric and adult patients.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Cardiac Arrest, Out-Of-Hospital

Interventions

AED 3 with Uni-padzDEVICE

Use of AED 3 with Uni-padz by lay rescuer

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * Suspected out-of-hospital cardiac arrest * Use of ZOLL AED 3 public-access defibrillator (running software v.1.03.602 or newer (US) or v. 6.03.006 or newer(OUS)) with Uni-padz III * Unconsciousness * Absence of breathing * Absence of pulse and other signs of circulation Exclusion Criteria: * Pre-existing Do Not Attempt Resuscitation (DNAR) orders * No evidence of cardiac arrest

Locations (2)

University at Buffalo

Buffalo, New York, United States

Colonie EMS

Latham, New York, United States

Outcomes

Primary Outcomes

CPR sensor placement

Rate of appropriate placement of the CPR electrodes and compression sensor

Time frame: Procedure (At time of device placement)

Selection of adult or pediatric mode

Rate of appropriate selection of child mode by pressing "Child Mode" button or adult mode by not pressing "Child Mode" button determined by energy level of first shock

Time frame: Procedure (At time of device placement)

Data from ClinicalTrials.gov

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