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RECRUITING
NCT04250857

HeartStart FRx Defibrillator Event Registry

Sponsor: Philips Clinical & Medical Affairs Global

View on ClinicalTrials.gov

Summary

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 Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

1400

Start Date

2019-11-04

Completion Date

2027-12

Last Updated

2025-02-26

Healthy Volunteers

Not specified

Interventions

DEVICE

HeartStart FRX

Automated External Defibrillator

Locations (1)

Philips

Monroeville, Pennsylvania, United States