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HeartStart HS1 Defibrillator* Event Registry

RECRUITINGSponsored by Philips Clinical & Medical Affairs Global
Actively Recruiting
SponsorPhilips Clinical & Medical Affairs Global
Started2021-02-25
Est. completion2027-12
Eligibility
Healthy vol.Accepted
Locations1 site
View on ClinicalTrials.gov →

NCT04840797

Summary

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

Eligibility

Healthy volunteers accepted
Inclusion Criteria:

* 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

Exclusion Criteria:

* 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.

Conditions2

Heart DiseaseSudden Cardiac Arrest

Locations1 site

Philips
Pittsburgh, Pennsylvania, 15206
Chase Wennick617-398-7347chase.wennick@philips.com

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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