I25.1
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: known or suspected CAD; especially including patients with thoracic pain, dyspnea on exertion, pathologic findings in an ergometry, resting ECG, echocardiography, or non-invasive ischemia testing (e.g., cardiac MRI or nuclear cardiac examinations)
Exclusion criteria
Exclusion criteria: pregnancy/lactation, acute coronary syndrome (ACS), status post bypass or other cardiac surgery, decompensated heart failure, valvular heart disease of higher degree, atrial fibrillation, other cardiac arrhythmia of higher degree, other clinically significant concomitant diseases, inability to follow procedures, insufficient knowledge of project language, inability to give consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary Endpoint is the diagnostic accuracy of SCG/GCG (seismocardiography/gyrocardiography) for the diagnostics of coronary artery disease in comparison with catheter/CT coronary angiography. SCG/GCG measurements will take place shortly before the clinical standard diagnostic procedure (i.e., catheter/CT coronary angiography), which serves as the gold standard. The comparison of SCG/GCG results with the gold standard and the statistical evaluation thereof will take place at the end of the study. The results of the clinical diagnostics will be taken from the clinical standard documentation (report of the coronary angiography). The results of SCG/GCG measurements will be documented on paper and electronically, the SCG/GCG data will be saved electronically. | — |
Countries
Switzerland
Contacts
UniversitätsSpital Zürich