Effect of Permanent Internal Mammary Artery Occlusion on Extracardiac Coronary Collateral Supply
IMAO
1 other identifier
interventional
50
1 country
1
Brief Summary
Coronary artery disease and the benefit of bypasses: Despite considerable advances in medicine, cardiovascular diseases remain the number one cause of death globally, primarily consequence of myocardial infarction (MI). Coronary collaterals exert a protective effect by providing an alternative source of blood flow to a myocardial territory potentially affected by an acute coronary occlusion. Coronary collaterals represent pre-existing inter-arterial anastomoses and as such are the natural counter-part of surgically created bypasses. Sufficient coronary collaterals have been shown to confer a significant benefit in terms of overall mortality and cardiovascular events. In this regard, the concept of augmenting coronary collateral function as an alternative treatment strategy to alter the course of CAD, as well as to control symptoms, is attractive. Durable promotion of coronary collateral circulation: Before the advent of coronary artery bypass grafting, permanent augmentation of coronary collateral supply by a single structural modification has already been attempted. Bilateral ligation of the internal mammary arteries (IMA) was performed in CAD patients to alleviate angina pectoris and electrocardiographic (ECG) signs of ischemia. The prevalent in vivo function of natural IMA-to-coronary artery bypasses and their anti-ischemic effect has - for the first time - been recently demonstrated by our research group. The acute functional changes observed in response to temporary distal IMA balloon occlusion are expected to result in larger chronic structural adaptations of the IMA-to-coronary-artery connections when the distal IMA is permanently occluded. In contrast to the previously employed arteriogenic approaches in humans, the attractiveness of such an intervention lies in the potential durability of the effect. In a first step, catheter-based IMA occlusion ought to be conceptually investigated in the setting of the less frequently grafted right IMA among patients with ischemia in the right coronary artery territory.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_1
Started Dec 2014
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2014
CompletedFirst Submitted
Initial submission to the registry
January 5, 2015
CompletedFirst Posted
Study publicly available on registry
June 18, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2016
CompletedMay 12, 2016
June 1, 2015
1.2 years
January 5, 2015
May 10, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change from baseline in right coronary Collateral Flow Index (CFI)
Change from baseline in right coronary Collateral Flow Index (CFI) at follow-up (week 6) vs baseline
Follow-up (week 6)
Secondary Outcomes (4)
Change from baseline in left coronary CFI
Follow-up (week 6)
Change from baseline in intracoronary and surface ECG ST-segment shift during temporary right and left coronary balloon occlusion
Follow-up (week 6)
Number of patients with angiographic visibility of right IMA-to-coronary anastomoses
Follow-up (week 6)
Number of patients with catheter-based permanent right IMA occlusion
Baseline, Follow-up (week 6)
Study Arms (1)
Interventional Study Arm
EXPERIMENTALIn the presence of a significant right coronary artery stenosis, catheter-based occlusion of the right IMA distal to the take-off of the pericardio-phrenic branch is performed at baseline using a dedicated occlusion device (Amplatzer vascular plug).
Interventions
Eligibility Criteria
You may qualify if:
- Age \> 18 years
- Referred for elective coronary angiography
- Written informed consent to participate in the study
- Significant stenosis of right coronary artery (FFR ≤0.80)
You may not qualify if:
- Acute coronary syndrome; unstable cardiopulmonary conditions, unstable angina pectoris
- Collateral flow index of right IMA \<0.25
- Severe cardiac valve disease
- Congestive heart failure NYHA III-IV
- Prior coronary artery bypass surgery / prior cardiac surgery
- Coronary artery disease best treated by coronary artery bypass grafting
- Coronary artery disease unsuitable for intracoronary pressure measurements
- Prior Q-wave myocardial infarction in the vascular territory undergoing collateral function determination
- Severe renal or hepatic failure
- Women of childbearing age
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bern University Hospital
Bern, 3010, Switzerland
Related Publications (4)
Stoller M, de Marchi SF, Seiler C. Function of natural internal mammary-to-coronary artery bypasses and its effect on myocardial ischemia. Circulation. 2014 Jun 24;129(25):2645-52. doi: 10.1161/CIRCULATIONAHA.114.008898. Epub 2014 Apr 17.
PMID: 24744276BACKGROUNDMoberg A. Anastomoses between extracardiac vessels and coronary arteries. II. Via internal mammary arteries. Post-mortem angiographic study. Acta Radiol Diagn (Stockh). 1967 May;6(3):263-72. doi: 10.1177/028418516700600306. No abstract available.
PMID: 6025072BACKGROUNDBLAIR CR, ROTH RF, ZINTEL HA. Measurement of coronary artery blood-flow following experimental ligation of the internal mammary artery. Ann Surg. 1960 Aug;152(2):325-9. doi: 10.1097/00000658-196008000-00018. No abstract available.
PMID: 13801236BACKGROUNDStoller M, Seiler C. Effect of Permanent Right Internal Mammary Artery Closure on Coronary Collateral Function and Myocardial Ischemia. Circ Cardiovasc Interv. 2017 Jun;10(6):e004990. doi: 10.1161/CIRCINTERVENTIONS.116.004990.
PMID: 28566292DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Seiler Christian, MD, Prof
Bern University Hospital
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NA
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 5, 2015
First Posted
June 18, 2015
Study Start
December 1, 2014
Primary Completion
March 1, 2016
Study Completion
April 1, 2016
Last Updated
May 12, 2016
Record last verified: 2015-06