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Diagnostic Validation of Wearable ECG Monitoring Patch, ATP-C120

Diagnostic Validation of Wearable Continuous ECG Monitoring Patch, ATP-C120, in High Risk Patients for New-onset Atrial Fibrillation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04857268
Enrollment
320
Registered
2021-04-23
Start date
2020-11-13
Completion date
2023-12-31
Last updated
2021-04-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation New Onset

Keywords

Arrhythmia, Atrial Fibrillation, Wearable Electronic Device

Brief summary

A new wearable patch-type device, ATP-C120 (ATsens, Seongnam, Korea) is a novel, single-lead ECG monitoring device and can continuously monitor the ECG signal for upto 11 days. This study is designed to experiment its diagnostic capability of new-onset atrial fibrillation in high risk patients. Several studies reported that validated CHA2DS2-VASc score has high performance in predicting new-onset atrial fibrillation and there are over 10 percent of new-onset atrial fibrillation in patients whose calculated CHA2DS2-VASc scores are ≥ 2. Thus, through this study, the investigators sought to evaluate the validation of early detection of new-onset atrial fibrillation by ATP-C120.

Detailed description

The prevention of stroke associated with atrial fibrillation is a leading global health concern. This devastating event is largely preventable with anticoagulant therapy. Therefore, the early detection and accurate diagnosis of arrhythmia are crucial for prevention of adverse outcome. However, because atrial fibrillation is often intermittent and mostly asymptomatic, it is difficult to capture an excise event. Conventional electrocardiogram (ECG) monitoring devices including multi-lead portable ECG monitoring device, event-detection monitoring device, and implantable ECG monitoring device are useful for early detection of atrial fibrillation, but these devices have various drawbacks such as requirement of multiple out-patient visits and need of invasive implantation of devices. A new wearable patch-type device, ATP-C120 (ATsens, Seongnam, Korea) is a novel, single-lead ECG monitoring device and can continuously monitor the ECG signal for upto 11 days. It has recently demonstrated its diagnostic capability and safety compared to the conventional ECG monitoring systems . Yet, it has not widely used in real-world. So, this study is designed to experiment its diagnostic capability of new-onset atrial fibrillation in high risk patients. Several studies reported that validated CHA2DS2-VASc score has high performance in predicting new-onset atrial fibrillation and there are over 10 percent of new-onset atrial fibrillation in patients whose calculated CHA2DS2-VASc scores are ≥ 2. Thus, through this study, the investigators sought to evaluate the validation of early detection of new-onset atrial fibrillation by ATP-C120.

Interventions

DEVICEwearable continuous ECG monitoring patch, ATP-C120

ATP-C120 is a novel, single-lead ECG monitoring device which can continuously monitor the ECG signal as long as 14 days (11 days if the device is connected to the smartphone via Bluetooth) when attached to skin adjacent to the heart of patients. It weighs about 8.3 g, with a size of 84 × 39 × 8.3 mm. When the device is attached to the patient, several predefined methods were utilized to prevent the occurrence of noise or signal loss. First, the skin was cleansed and disinfected using a 70% ethanol solution. Skin hair was removed if needed. Then the protection film was removed from the patient-side surface of the device. The device is placed at the left 3rd intercostal space 45 degrees tilted toward the inside.

Sponsors

Kyungpook National University Hospital
CollaboratorOTHER
Seoul National University Bundang Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. patients who provide written and informed consent to participate 2. patients whose calculated CHA2DS2-VASc score is ≥ 2

Exclusion criteria

1. subjects previously diagnosed with atrial fibrillation 2. subjects implanted pacemaker, cardioverter-defibrillator, or any electrical devices 3. subjects had skin problems such as allergic contact dermatitis 4. female patients who are pregnant, or lactating status.

Design outcomes

Primary

MeasureTime frameDescription
Rate of new-onset atrial fibrillation11 daysnew-onset atrial fibrillation recognized by ATP-C120 patch device

Secondary

MeasureTime frameDescription
Rate of new-onset atrial fibrillation6 monthnew-onset atrial fibrillation recognized by conventional ECG monitoring device

Countries

South Korea

Contacts

Primary ContactJu-Seung Kwun, MD.
jkwun0413@gmail.com+82-10-9279-5372
Backup ContactGa-hyun Lee, RN
R2631@snubh.org+82-10-2534-3761

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026