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Evaluation and comparison of Duration parameters and Amplitudes parameters of Spandan PRO ECG machine

Not Applicable
Registration Number
CTRI/2024/07/070766
Lead Sponsor
Sunfox Technologies Private Limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All IPD and OPD patients referred by the cardiologist for ECG tests in the ECG laboratory will be included

Exclusion Criteria

Subjects aged below 20 years were excluded from the study.

ECG reports with underlying electrical disturbances and motion artifacts were also excluded.

Pregnant females.

Individuals with loosened skin and high density of chest hairs.

The device is not to be used with a defibrillator.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
determine the equivalency of the smartphone ECG device in comparison to the Goldstandard ECG machine for measuring the morphological parameters like PR intervals and QRS duration under the Clinical level of Agreement and less margin of error <br/ ><br>Timepoint: 2 weeks
Secondary Outcome Measures
NameTimeMethod
To access the feasibility <br/ ><br>and usability of the smartphone based ECG device in accessing the ECG from the patients & also to evaluate its accuracy when used in ECG room.Timepoint: 2 Months
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