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Not yet recruiting NCT06360224

Collect Flow and Ultrasound Images of Coronary Bypass Grafts

— Observational Cardiac Bypass Surgery (CABG)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: MiraQ systems with Transit Time Flow Measurement (TTFM) and High Frequency Ultrasound (HFUS) probes.
Who it may be relevant to
Registry conditions: Cardiac Bypass Surgery (CABG). Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

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).

Interventions

  • Device MiraQ systems with Transit Time Flow Measurement (TTFM) and High Frequency Ultrasound (HFUS) probes
    The objective of this study is to harvest a wide dataset of high quality to allow exploratory analysis and training of machine learning

Primary outcome measures

  • Wide and high-quality dataset uploaded to CaseCloud from CABG-procedures. [Time frame: 1 day]

Eligibility criteria

Inclusion criteria

  • 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

Exclusion criteria

  • Patient younger than 18 years
  • Any condition that the investigator believes should exclude participation

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06360224 · CASES

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗