About this trial
This is a post-market observational, non-interventional, multicenter clinical investigation with the purpose of harvesting high quality data from regular cardiac bypass surgery (CABG).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patient older than 18 years
Scheduled for CABG
Understand the nature of the procedure and willingness to comply with the CIP
Provide written informed consent
Disqualifiers
Patient younger than 18 years
Any condition that the investigator believes should exclude participation
Trial population
Patients scheduled for cardiac bypass surgery (CABG) that have signed an informed consent form for this study
Trial design
Other
Prospective
Treatments tested in this trial
MiraQ systems with Transit Time Flow Measurement (TTFM) and High Frequency Ultrasound (HFUS) probes
DeviceThe objective of this study is to harvest a wide dataset of high quality to allow exploratory analysis and training of machine learning
Treatment groups
Trial outcomes
Primary outcomes
Wide and high-quality dataset uploaded to CaseCloud from CABG-procedures.
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: