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NCT Number: NCT06360224

Collect Flow and Ultrasound Images of Coronary Bypass Grafts

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).

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Key information

Conditions

Cardiac Bypass Surgery (CABG)

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

MiraQ systems with Transit Time Flow Measurement (TTFM) and High Frequency Ultrasound (HFUS) probes

Device

The objective of this study is to harvest a wide dataset of high quality to allow exploratory analysis and training of machine learning

Primary outcomes

  1. Wide and high-quality dataset uploaded to CaseCloud from CABG-procedures.

    Time frame: 1 day

Study contacts

Contact information is provided by the study sponsor or research team.

Haakon Grøthe

CONTACT

[email protected]

04790968263

Sponsors and collaborators

Lead sponsor

Medistim ASA

Industry

Registry information

Acronym: CASES

Important dates

Study start
2024
Primary completion
2029
Study completion
2029
First posted
Apr 11, 2024
Registry last updated
Apr 11, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.