Evaluation of Effectiveness and Safety of Hybrid Coronary Revascularization

  • STATUS
    Recruiting
  • End date
    Dec 27, 2030
  • participants needed
    200
  • sponsor
    Seung-Jung Park
Updated on 27 January 2021
coronary revascularization

Summary

This study evaluated the effectiveness and safety of Hybrid Coronary Revascularization in real-world practice.

Details
Condition Coronary artery bypass graft, Coronary Artery Stenosis, Percutaneous Coronary Intervention, Coronary Artery Disease Progression, Percutaneous Coronary Revascularization, cabg, coronary artery bypass, coronary bypass, coronary artery bypass surgery, coronary stenosis
Treatment Hybrid Coronary Revascularization
Clinical Study IdentifierNCT03788369
SponsorSeung-Jung Park
Last Modified on27 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age greater than or equal to 20 yrs?
Gender: Male or Female
Do you have any of these conditions: Coronary Artery Disease Progression or Coronary Artery Stenosis or Coronary artery bypass graft or Percutaneous Coronary Revascularization?
Do you have any of these conditions: Percutaneous Coronary Intervention or Percutaneous Coronary Revascularization or coronary artery bypass or Coronary artery bypass graft or coronary st...?
Do you have any of these conditions: coronary bypass or Coronary artery bypass graft or Percutaneous Coronary Revascularization or cabg or Percutaneous Coronary Intervention or Coronary A...?
Do you have any of these conditions: Coronary Artery Disease Progression or cabg or Percutaneous Coronary Intervention or Coronary artery bypass graft or coronary artery bypass surgery or...?
Age 20 and more
Hybrid coronary revascularization due to multivessel coronary artery disease(must include left anterior descending artery)
Written consent

Exclusion Criteria

Previous CABG(coronary artery bypass graft)
Life expectancy 1 year
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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