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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
124
unshielded device measuring cardiac magnetic fields
Icahn School of Medicine at Mount Sinai
New York, New York, United States
% analyzable Sandbox MCG data
% Sandbox MCG data collected and suitable for analysis
Time frame: during the procedure (MCG scan)
Sandbox MCG safety
Device-related adverse events
Time frame: 30 days
Characterization of scan results that may differentiate between high risk and low risk ACS patients
Signal Noise Ratio of ECG features
Time frame: during the procedure (MCG scan)
Characterization of scan results that may differentiate between high risk and low risk ACS patients
t-wave field maximum angle
Time frame: during the procedure (MCG scan)
Characterization of scan results that may differentiate between high risk and low risk ACS patients
heartbeats needed to obtain signal
Time frame: during the procedure (MCG scan)
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