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MCG Discovery Study in Emergency Departments

NCT06095557 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 124

Last updated 2025-10-21

No results posted yet for this study

Summary

This prospective discovery study is designed to demonstrate the feasibility of using an unshielded, mobile MCG device in an Emergency Department (ED) setting. The main question it aims to answer is whether interpretable data can be reliably collected as part of an ED workflow.

Conditions

  • ACS - Acute Coronary Syndrome
  • NSTEMI - Non-ST Segment Elevation MI

Interventions

DEVICE

Sponsor MCG device

unshielded device measuring cardiac magnetic fields

Sponsors & Collaborators

  • SB Technology, Inc.

    lead INDUSTRY

Principal Investigators

  • Kit Yee Au-Yeung, PhD · SB Technology, Inc.

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-30
Primary Completion
2025-06-09
Completion
2025-07-08
FDA Device
Yes

Countries

  • United States

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 NCT06095557 on ClinicalTrials.gov