Clinical Efficacy of Permanent Internal Mammary Artery Occlusion in Stable Coronary Artery Disease
Coronary Artery Disease, Internal Mammary-Coronary Artery Anastomosis, Ischemia
About this trial
This is an interventional treatment trial for Coronary Artery Disease focused on measuring Collateral Flow Index, Permanent Internal Mammary Artery Occlusion
Eligibility Criteria
Inclusion Criteria:
- Chronic stable 1- to 3-vessel CAD
- Written informed consent to participate in the study
Exclusion Criteria:
- Absence of at least one coronary stenotic lesion ≥50% diameter narrowing.
- Acute coronary syndrome; unstable cardiopulmonary condition, unstable angina pectoris
- Severe valvular heart disease
- Congestive heart failure NYHA III-IV
- Prior coronary artery bypass surgery / prior cardiac surgery
- CAD best treated by coronary artery bypass grafting
- Prior Q-wave myocardial infarction in the vascular territory undergoing collateral function measurement
- Severe renal or hepatic failure
- Women of childbearing age
Sites / Locations
- University Hospital Inselspital, Bern
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
Intervention
Sham-Control
In the presence of a significant coronary artery stenosis and randomization to the intervention group: Catheter-based permanent occlusion of the ipsilateral (to the culprit coronary lesion) IMA will be performed at the projected height of inferior vena cava confluence and right atrium using a dedicated occlusion device (Amplatzer vascular plug 4, CE0086).
In the presence of a significant coronary artery stenosis, and randomization to the sham-procedure: IMA will be selectively intubated using an appropriate catheter. Angiography of the IMA and the pericardiacophrenic branch will be performed.