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Anonymized Data Collection From the CS6BP for Heart Arrythmias Measurements

NCT05723744 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 47

Last updated 2023-02-13

No results posted yet for this study

Summary

The purpose of this clinical study is to collect data simultaneously with the CS6BP watch sensors during EPS in order to characterize different evoked arrhythmias and record Blood Pressure during the procedures that blood pressure is collected by an automated cuff.

Conditions

  • Heart Arrythmias

Interventions

DEVICE

ECG Holter and investigational device recordings for the purpose of developing Continuous Measurement of Heart Arrythmias

For Candidates for pacemaker implantation: ECG Holter and investigational device recordings (of PPG, ECG, and motion sensors tracings non-invasively) will be recorded before procedure, during patient's hospitalization at cardiology division. Blood pressure values that are collected by an automated cuff will be collected including any notes attached to the values. All collected data will be analyzed offline

Sponsors & Collaborators

  • CardiacSense Ltd.

    lead INDUSTRY

Principal Investigators

  • Aharon Abbo, MD · Rambam Health Care Campus

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-11-27
Primary Completion
2023-02-01
Completion
2023-02-01

Countries

  • Israel

Study Locations

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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 NCT05723744 on ClinicalTrials.gov