Left Ventricular Systolic Dysfunction Clinical Trial
Official title:
A Study to Evaluate Accuracy and Validity of the "Chang Gung" Ventricular Systolic Dysfunction Screening Software
Verified date | May 2023 |
Source | Chang Gung Memorial Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this research is to test a software tool called the "Chang Gung" Ventricular Systolic Dysfunction screening software, which uses a 12-lead electrocardiogram to determine if a patient has left ventricular systolic dysfunction. The goal is to determine if the software can accurately identify patients with this condition, which would help doctors diagnose and treat it more effectively. The trial will involve using the software on patients and comparing its results to those obtained through echocardiograms, which are currently the gold standard for diagnosing left ventricular systolic dysfunction. Only patients who meet specific eligibility criteria will be able to participate in the trial, and the software will be administered by trained healthcare professionals. The study will help determine if the software is a useful tool for diagnosing left ventricular systolic dysfunction, which could lead to earlier diagnosis and better outcomes for patients. The research team will collect and analyze data on the accuracy of the software and its usability in clinical practice. Overall, this study will provide important information for doctors and patients about a new tool for diagnosing left ventricular systolic dysfunction.
Status | Completed |
Enrollment | 1172 |
Est. completion date | October 2, 2023 |
Est. primary completion date | August 15, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 100 Years |
Eligibility | Inclusion Criteria: - Equal or greater than twenty years old. - Static 12-lead electrocardiogram of General Electric MUSE XML format file. - The data comes from the static 12-lead electrocardiogram device of General Electric (model MAC5500). - Echocardiography data within 14 days before or after the electrocardiogram acquisition time. - The electrocardiogram signal is 500 Hz. - The Alternating current (AC) filter of the electrocardiogram signal is 60 Hz. - The length of the electrocardiogram signal is ten seconds (the electrocardiogram output of model MAC5500 is ten seconds, and there is no need to capture a segment). Exclusion Criteria: - Cases used in the model development process. - Lacks any electrode. - Contain any electrode lacks a segment. |
Country | Name | City | State |
---|---|---|---|
Taiwan | Chang Gung memorial hospital | Taoyuan City |
Lead Sponsor | Collaborator |
---|---|
Chang Gung Memorial Hospital |
Taiwan,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Sensitivity | The rate of test results that correctly indicate the presence. | baseline | |
Secondary | Specificity | The rate of test results that correctly indicate the absence. | Baseline | |
Secondary | Accuracy | The rate of all test results that correctly indicated. | Baseline | |
Secondary | Area Under the receiver operating characteristic Curve | A graphical plot that illustrates the diagnostic ability of a binary classifier system as its discrimination threshold is varied. | Baseline | |
Secondary | Positive predictive value | The proportions of positive results in statistics and diagnostic tests that are true positive results | Baseline | |
Secondary | Negative predictive value | The proportions of negative results in statistics and diagnostic tests that are true negative results | Baseline | |
Secondary | False positive rate | The rate of test result which wrongly indicates that a particular condition or attribute is present | Baseline | |
Secondary | False negative rate | The rate of test result which wrongly indicates that a particular condition or attribute is absent | Baseline |
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