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A Usability Study of a Multi-channel ECG Monitoring Device

NCT07388355 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 500

Last updated 2026-02-05

No results posted yet for this study

Summary

This study it to evaluate the usability of the WearLinq eWave patch in a general adult population.

Conditions

Interventions

DEVICE

eWave Patch

This device is a wearable multi-channel ECG monitoring device for continuous cardiac rhythm tracking.

Sponsors & Collaborators

  • ABio Clinical Research Partners

    collaborator UNKNOWN

  • Wearlinq

    lead INDUSTRY

Principal Investigators

  • Chris Daniel · WearLinq, Inc.

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-02-28
Primary Completion
2027-12-31
Completion
2027-12-31
FDA Device
Yes

Countries

  • United States

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 NCT07388355 on ClinicalTrials.gov