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A Wearable With Photoplethysmography and 6-lead Electrocardiography for Atrial Fibrillation Detection

NCT04281927 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 435

Last updated 2021-02-10

No results posted yet for this study

Summary

A single center prospective case-control study to evaluate ability of a wearable to differentiate between atrial fibrillation (AF) and sinus rhythm (SR).

Conditions

Interventions

DEVICE

Monitoring with wearable (the tested device) and Holter ECG (eMotion Faros 90)

Participants will use the wearable (the tested device) to record at least 2 minutes of photoplethysmography and 6-lead ECG. In addition, each subject will be monitored with synchronous ECG Holter monitoring (with eMotion Faros 90).

Sponsors & Collaborators

  • Kaunas University of Technology

    collaborator OTHER

  • Vilnius University

    lead OTHER

Principal Investigators

  • Audrius Aidietis, Prof. PhD · Vilnius University

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-03-06
Primary Completion
2019-11-15
Completion
2019-11-15

Countries

  • Lithuania

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04281927 on ClinicalTrials.gov