HeartStart HS1 Defibrillator* Event Registry

Recruiting now

Conditions studied: Sudden Cardiac Arrest

In brief

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

Key facts

Study ID

NCT04840797

Run by

Philips Clinical & Medical Affairs Global

People needed

1400

Starts

2021-02-25

Expected to finish

2027-12-01

Last updated by the study team

2025-02-26

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Have been suspected of a circulatory arrest for any cause.
• Have had HeartStart HS1 Defibrillator with electrodes:
• Adult SMART Pads Cartridge [REF: M5071A], Infant/Child SMART Pads Cartridge (REF:M5072A) applied to their body and powered up with HS1 battery (Model M5070A), regardless of whether a defibrillation shock was delivered

You may not qualify if…

• 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.

Where it is running

• Philips — Pittsburgh, Pennsylvania, United States (enrolling)

Full record on ClinicalTrials.gov

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