Ignite Creation Date:
2024-07-17 @ 11:16 AM
Last Modification Date:
2024-10-26 @ 3:32 PM
Study NCT ID:
NCT06471764
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-06-24
First Post:
2024-06-18
Brief Title:
Validation Study of Frontier X Plus FX Device
Sponsor:
Fourth Frontier Technologies Pvt Ltd
Organization:
Fourth Frontier Technologies Pvt Ltd
Study Overview
Official Title:
Validation Study of Frontier X Plus FX Device Recording an Electrocardiogram ECG for Retrospective Rhythm Analysis in Patients with and Without Atrial Fibrillation AF in US Subjects
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The main objective of this study is to validate the specificity and sensitivity of FX detecting atrial fibrillation AF in both AF and non-AF subjects using a comparative approach which involves using both a US FDA-cleared gold standard 12-lead and a consumer device which stores ECG FX2 consumer model used to store the ECG for analysis retrospectively
The results obtained from this clinical investigation will serve as evidence for larger clinical investigation designs for this non-invasive and fully mobile method of continuous AF measurement in the adult population including those with known or unknown cases of AF The ultimate goal of this study is to establish the effectiveness of this novel approach in detecting and monitoring AF which could potentially revolutionize the field of remote cardiac monitoring and improve the quality of care for patients with AF and other cardiac arrhythmias
The results obtained from this clinical investigation will serve as evidence for larger clinical investigation designs for this non-invasive and fully mobile method of continuous AF measurement in the adult population including those with known or unknown cases of AF The ultimate goal of this study is to establish the effectiveness of this novel approach in detecting and monitoring AF which could potentially revolutionize the field of remote cardiac monitoring and improve the quality of care for patients with AF and other cardiac arrhythmias
Detailed Description:
Atrial Fibrillation AF patients frequently require hospitalization medications and anticoagulation therapy all of which can be costly Moreover living with and caring for AF patients can also be challenging as the condition can cause physical emotional and financial stress for both patients and their caregivers There are many published studies on non-invasive ECG monitoring devices and their benefits for patients with Atrial fibrillation One study published in the Journal of the American College of Cardiology found that wearable ECG monitors can increase the detection of atrial fibrillation and potentially reduce the risk of stroke Easy-to-use devices like FX with their ability to continuously record high-quality ECGs can aid monitoring without interrupting activities of daily living and can support more patient-involved self-management care that integrates education engagement and shared decision-making thereby allowing for a significant improvement in their quality of life and a reduction in healthcare utilization
There is an evolving belief that these wireless monitoring devices will mark a new era in medicine and a transition from population-level health care to individualized medicine in which suitable patients are equipped with advanced biosensors that in turn have their data processed through sophisticated algorithms to predict events before or leading to their occurrence
The ECG is a measurement of the electrical activity of the heart Each 20-second segment of the ECG data can be automatically analyzed for arrhythmia detection which is classified into one of 6 categories normal sinus rhythm atrial fibrillation bradycardia tachycardia inconclusive unreadable
The FX weighs 20 grams and gets mounted on a chest strap embedded with ECG sensors It has advanced miniaturized sensors with onboard computing and wireless connectivity to enable the device to obtain and analyze ECG signals from the HeartKey ECG algorithm FX helps create record store transfer and display a single-channel electrocardiogram ECG like a Lead-I ECG The Frontier X Plus will determine the presence of atrial fibrillation AF and sinus rhythm on a classifiable waveform Please note for this study an FX2 consumer non-medical version with identical hardware will be utilized with modified firmware to collect data on the ECG rhythm status but not communicate it to the user or patient For the purposes of the protocol the test device is referred to as the FX
FX is equipped with a Bluetooth Low Energy Transmitter which can communicate with a mobile application and control the data acquisition displaying the status of the device heart rate and breathing rate Optionally the ECG waveform can be viewed in real-time on the mobile app during a live streaming session for assessing signal quality The mobile App Android and iOS also stores the ECG and related information arrhythmia information and relays it to a cloud server for permanent storage and review by healthcare staff or investigators The Frontier Plus Mobile application determines the presence of various types of rhythm on a classifiable waveform as indicated in the Table above The device is for prescription use and the user is not intended to interpret or take clinical action based on the device output without consultation with a qualified healthcare professional The ECG waveform will be intended to supplement rhythm classification to discriminate AF from sinus rhythm and is not intended to replace traditional methods of diagnosis or treatment
There is an evolving belief that these wireless monitoring devices will mark a new era in medicine and a transition from population-level health care to individualized medicine in which suitable patients are equipped with advanced biosensors that in turn have their data processed through sophisticated algorithms to predict events before or leading to their occurrence
The ECG is a measurement of the electrical activity of the heart Each 20-second segment of the ECG data can be automatically analyzed for arrhythmia detection which is classified into one of 6 categories normal sinus rhythm atrial fibrillation bradycardia tachycardia inconclusive unreadable
The FX weighs 20 grams and gets mounted on a chest strap embedded with ECG sensors It has advanced miniaturized sensors with onboard computing and wireless connectivity to enable the device to obtain and analyze ECG signals from the HeartKey ECG algorithm FX helps create record store transfer and display a single-channel electrocardiogram ECG like a Lead-I ECG The Frontier X Plus will determine the presence of atrial fibrillation AF and sinus rhythm on a classifiable waveform Please note for this study an FX2 consumer non-medical version with identical hardware will be utilized with modified firmware to collect data on the ECG rhythm status but not communicate it to the user or patient For the purposes of the protocol the test device is referred to as the FX
FX is equipped with a Bluetooth Low Energy Transmitter which can communicate with a mobile application and control the data acquisition displaying the status of the device heart rate and breathing rate Optionally the ECG waveform can be viewed in real-time on the mobile app during a live streaming session for assessing signal quality The mobile App Android and iOS also stores the ECG and related information arrhythmia information and relays it to a cloud server for permanent storage and review by healthcare staff or investigators The Frontier Plus Mobile application determines the presence of various types of rhythm on a classifiable waveform as indicated in the Table above The device is for prescription use and the user is not intended to interpret or take clinical action based on the device output without consultation with a qualified healthcare professional The ECG waveform will be intended to supplement rhythm classification to discriminate AF from sinus rhythm and is not intended to replace traditional methods of diagnosis or treatment
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None