HeartStart HS1 Defibrillator* Event Registry

Description

A Prospective study on the performance and safety of the HeartStart OnSite (Model M5066A) \& HeartStart Home (Model M5068A) Defibrillator device data.

Conditions

Sudden Cardiac Arrest

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Study Overview

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Study Details

Study overview

A Prospective study on the performance and safety of the HeartStart OnSite (Model M5066A) \& HeartStart Home (Model M5068A) Defibrillator device data.

HeartStart HS1 Defibrillator* Event Registry

HeartStart HS1 Defibrillator* Event Registry

Condition
Sudden Cardiac Arrest
Intervention / Treatment

-

Contacts and Locations

Pittsburgh

Philips, Pittsburgh, Pennsylvania, United States, 15206

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Have been suspected of a circulatory arrest for any cause.
  • * Have had HeartStart HS1 Defibrillator with electrodes:
  • * Subjects will be excluded if any of the following are present:
  • * AED or pad use other than the HeartStart HS1 Defibrillator with above referenced Philips electrode pads. Note: Use of a device other than the Philips HeartStart HS1 AED does not preclude enrollment if the AED or an Advanced Life Support defibrillator was used after the HeartStart HS1 AED.
  • * AED used for training purposes.

Ages Eligible for Study

to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Philips Clinical & Medical Affairs Global,

Gerrit Noordergraaf, MD PhD, PRINCIPAL_INVESTIGATOR, Philips Healthcare

Study Record Dates

2027-12