Clinical Research Directory
Browse clinical research sites, groups, and studies.
HeartStart FRx Defibrillator Event Registry
Sponsor: Philips Clinical & Medical Affairs Global
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
Conditions
Interventions
HeartStart FRX
Automated External Defibrillator
Locations (1)
Philips
Monroeville, Pennsylvania, United States