Validation of ECG Waveform and Arrhythmia Diagnosis Concordance for Pediatric Patients Using ECG Monitoring Patch

Sponsor
Mezoo Co., Ltd. (Other)
Overall Status
Recruiting
CT.gov ID
NCT05756309
Collaborator
(none)
105
1
1
10.4
10.1

Study Details

Study Description

Brief Summary

This study will verify the 1-channel patch-type ECG's arrhythmia diagnostic concordance rate and electrocardiogram measurement performance in pediatric patients by collecting ECG signals from patch-type ECG and Holter device simultaneously for data analysis.

Condition or Disease Intervention/Treatment Phase
  • Device: Electrocardiogram measurements by holter device and patch-type electrocardiographic at the same time
N/A

Detailed Description

[How to conduct research] This study targeted more than 29 days old and less than 19 years old. Written consent is obtained from those who need a Holter examination among outpatients or inpatients at the Pediatrics of Samsung Medical Center. The medical staff attaches the Holter device to the subject and the patch-type electrocardiograph in the Holter examination room. Holter device and patch-type electrocardiograph are returned to the Holter examination room after measuring the electrocardiogram for 24 hours. ECG signals from patch-type electrocardiographs and commercial Holter device and arrhythmia detection information are compared and analyzed.

[Number of Subjects] The number of this study is 105. Written consent is obtained from those who need a Holter examination among outpatients or inpatients at the Pediatrics.

[Data analysis plan] In this study, the personal identification information of the subjects will be coded non-identifying and the collected electrocardiogram data will be stored in the cloud with restricted access from outsiders. Coded, non-identified research data is stored and managed in the cloud in compliance with privacy standards and information security standards. ECG data transmitted through the mobile application is stored in the cloud. Confidentiality and security of data are guaranteed, and data collected from patch-type electrocardiograph is used only for research. The electrocardiogram data acquired in this study are obtained in TXT or MAT format and used for data analysis.

The efficacy evaluation items are as follows.

  1. Comparison of ECG signal concordance

  2. Comparison of the parameters below for a noise-free section of about 1 minute, not the entire section

  • P-wave, QRS-complex, T-wave: Sensitivity, Positive Predictive Value, Amplitude difference, Correlation to the entire signal

  • P, QRS, T (On/Off time): Time difference

  • PR, QRS, QT (Duration/Interval): Time difference

  1. Comparison of arrhythmia diagnosis concordance rates between 24-hour patch-type electrocardiograph and commercial Holter device measurement data by arrhythmia categories (total of 19 including ventricular ectopic beat)

The evaluation method and interpretation method are as follows.

  1. In the case of categorical variables, the sensitivity and positive predictive value are evaluated, and in the case of continuous variables, the concordance between the measured values measured by the patch-type electrocardiograph and the Holter device is evaluated using the Bland-Altman plot.

  2. Amplitude difference of P-wave, QRS-complex and T-wave & Correlation to the entire signal

  • Peaks of P-wave, QRS-complex (R-wave peaks) and peaks of T-wave are manually annotated in the holter device and patch-type ECG independently to assess amplitude difference and correlation to the entire ECG signal.
  1. Time difference of P, QRS, T (On/Off time) & PR, QRS, QT (Duration/Interval)
  • Exact timing of fiducial markers such as onset of P-wave and QRS-complex, and offset of P-wave, QRS-complex, T-wave and clinically useful intervals and durations (PR-interval, RR interval, QT interval, P-wave duration, QRS-duration) are manually annotated in the holter device and patch-type ECG independently to quantify the accuracy of delineating these characteristic points in the patch sensor.
  1. Root Mean Square of Heart Rate
  • Calculate and analyze the square root after averaging the squares of each heart rate value in the analysis section from the electrocardiogram obtained simultaneously from the Holter device and the patch-type electrocardiograph

Study Design

Study Type:
Interventional
Anticipated Enrollment :
105 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Validation of Electrocardiogram Waveform, Heart Rate Accuracy and Arrhythmia Diagnosis Concordance for Pediatric Patients Using Single-channel ECG Monitoring Patch and Holter Monitoring
Actual Study Start Date :
Jan 16, 2023
Anticipated Primary Completion Date :
May 30, 2023
Anticipated Study Completion Date :
Nov 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Electrocardiogram measurements by holter device and patch-type electrocardiographic at the same time

The patient is measured electrocardiogram simultaneously through a holter device and patch-type electrocardiograph

Device: Electrocardiogram measurements by holter device and patch-type electrocardiographic at the same time
The patient is measured electrocardiogram simultaneously through a holter device and patch-type electrocardiograph

Outcome Measures

Primary Outcome Measures

  1. Comparison of arrhythmia diagnosis concordance rates between patch-type electrocardiograph and commercial Holter device measurement data by arrhythmia categories [Within 3 months after electrocardiogram procedure]

    Comparison of arrhythmia diagnosis concordance rates between 24-hour patch-type electrocardiograph and commercial Holter device measurement data by arrhythmia categories(total of 19 including ventricular ectopic beat)

  2. Comparison of ECG signal concordance between patch-type electrocardiograph and holter device [Within 3 months after electrocardiogram procedure]

    Calculate the concordance (%) of the ECG signal by comparing and analyzing total QRS complex, total ventricular ectopic beats, total atrial ectopic beats, minimum heart rate(bpm), maximum heart rate(bpm), average heart rate(bpm) and maximum RR interval(ms)

Eligibility Criteria

Criteria

Ages Eligible for Study:
29 Days to 19 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • More than 29 days old and less than 19 years old

  • Patients who are need regular Holter electrocardiography among outpatients or hospitalized patients at the Pediatrics, Samsung Medical Center

  • Those who gave written consent to this clinical study or obtained the written consent of the legal representative

Exclusion Criteria:
  • Patients who cannot give consent through the patient ownself or legal representative

  • If the researcher judges that participation in this study is inappropriate for other reasons

Contacts and Locations

Locations

Site City State Country Postal Code
1 Samsung Medical Center Seoul Korea, Republic of

Sponsors and Collaborators

  • Mezoo Co., Ltd.

Investigators

  • Study Director: Junghwan Park, CEO

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Mezoo Co., Ltd.
ClinicalTrials.gov Identifier:
NCT05756309
Other Study ID Numbers:
  • CDV-2022-02
First Posted:
Mar 6, 2023
Last Update Posted:
Mar 6, 2023
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Mezoo Co., Ltd.
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 6, 2023