HeartStart FRx Defibrillator Event Registry

Recruiting now

Conditions studied: Sudden Cardiac Arrest

In brief

This post market clinical follow-up study is a multi-center, non-randomized, unblinded, observational registry of the performance of the FRx Automated external defibrillator (AED) used in conjunction with electrodes with or without use of the infant/child key. The registry is focused only on on post-event data collection and does not prescribe any device usage. This registry has several safeguards in place to prevent against selections bias, including enrollment of all participants who have pads placed. This registry will evaluate the safety and verify the clinical performance of the device in relation to its claims, when used in accordance with the Device Manual.

Key facts

Study ID

NCT04250857

Run by

Philips Clinical & Medical Affairs Global

People needed

1400

Starts

2019-11-04

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…

• Subjects accepted into the study must: have been suspected of a circulatory arrest for any cause
• Have had HeartStart FRx AED with electrodes: HeartStart SMART PADS II applied to their body and powered up, regardless of whether a defibrillation shock was delivered

You may not qualify if…

• AED or pad use other than the HeartStart FRx AED with electrodes : HeartStart SMART PADS II
• AED used for training purposes.

Where it is running

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

Full record on ClinicalTrials.gov

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