Circulation, CollateralIMAORNCT03950947
Effect of Permanent Right Internal Mammary Artery Occlusion on Extracardiac Coronary Collateral Supply
A study testing Amplatzer vascular plug in people with Circulation, Collateral and Coronary Artery Disease, run by Insel Gruppe AG, University Hospital Bern at 1 site in Switzerland.
Trial 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). Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Circulation, Collateral, Coronary Artery Disease, Internal Mammary-Coronary Artery Anastomosis
- What is being tested?
- Amplatzer vascular plug
- Type of treatment
- Medical device
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 100 participants
- Where
- 1 siteSwitzerland
- Study dates
- 8 Jul 2016to 22 Feb 2019
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 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)
Who cannot join
- 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
Show all 10Show fewer
- 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
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Effect of Permanent Internal Mammary Artery Occlusion on Extracardiac Coronary Collateral Supply: a Randomized Controlled Study
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.
Read more
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 internal mammary arteries (IMA)-to-coronary artery bypasses and their anti-ischemic effect has been recently demonstrated by the investigators' research group. Levels of collateral function and myocardial ischemia were determined in a prospective, open-label clinical trial of permanent IMA device occlusion. In this study, coronary collateral function, has been shown to be augmented in the presence vs the absence of distal permanent ipsilateral IMA occlusion. These findings have been corroborated by the observed reduction in ischemia in the intracoronary ECG.
After this first step, the concept of permanent right IMA occlusion will be now investigated with a randomized, sham-controlled clinical trial.
Read the detailed description
Despite considerable advances in medicine, cardiovascular diseases remain the number one cause of death globally. In industrialized countries, coronary artery disease (CAD) is the leading cause of death, consequence of myocardial infarction (MI).
In patients with acute coronary syndrome, percutaneous coronary intervention (PCI) has been shown to improve outcomes. For chronic stable CAD, a recent meta-analysis including more than 93'000 patients has concluded that there may be "evidence for improved survival with new generation drug eluting stents but no other percutaneous revascularization technology compared with medical treatment" . Conversely, a current review of recently published meta-analyses and the detailed analyses of 3 widely quoted individual studies indicate no difference exists among stable CAD patients between PCI and medical therapy regarding nonfatal myocardial infarct or all-cause or cardiovascular mortality. A very recently published randomized controlled trial among patients with stable, single-vessel CAD, the so called ORBITA trial, has found that PCI of the stenotic lesion did not prolong exercise time by more than the effect of a sham procedure during the short observation period of 6 weeks.
In contrast, coronary artery bypass grafting (CABG) was superior to PCI in patients with diabetes and multivessel CAD. CABG significantly reduced rates of death and myocardial infarction compared to PCI, but at a higher rate of stroke. Furthermore, in patients with advanced CAD, rates of myocardial infarction were more than 60% lower with CABG compared to PCI.
Conceptually, the benefit of CABG over PCI is not surprising as PCI targets significant coronary lesions thought to be responsible for causing ischemia. However, the deleterious effects of atherosclerosis are not typically preceded by significant luminal vascular narrowing. The vulnerable plaque eventually becoming the culprit plaque (causing myocardial infarction or sudden cardiac death) has typically a relatively mild stenosis. Furthermore, due to being multifocal and widespread, plaque vulnerability is not a target for, nor amenable to PCI.
Conversely, artificial - or natural - bypasses 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 (i.e. coronary arteriogenesis) as an alternative treatment strategy of revascularization to alter the course of CAD is attractive. In particular, promotion of natural coronary bypasses is an appealing concept for patients with CAD not or not entirely treatable by the conventional coronary revascularization methods of PCI and CABG. According to an analysis by Williams et al, 142 of 493 patients with chronic stable CAD (29%) belonged to the group with incomplete coronary revascularization (partial and no revascularization plus the so called no-option group), and this group showed reduced survival during the 3-year follow-up period. Coronary collateral function promotion from any source could, thus, contribute to the completeness of myocardial revascularization. Incomplete coronary revascularization in chronic CAD has been shown in a very large (n=35'993 patients), recently published registry-based study to reduce overall survival according to the number of vessels not treated by PCI and according to the severity of stenoses left untreated. Coronary arteriogenesis, i.e., the growth of pre-existing collateral vessels has to occur well in advance of acute atherothrombotic coronary artery occlusion in order to limit infarct size. The source of blood supply via natural coronary bypasses (collateral arteries) to a circulatory area at risk for infarction can be within the coronary circulation, but also via extracardiac paths, e.g., via internal mammary arteries (IMA; also termed internal thoracic arteries). Extracardiac coronary artery supply is conceptually related to the term coronary collateral circulation because of its known anatomical structure as arterial anastomoses between, e.g., IMA, the pericardium and coronary arterial branches. In an editorial, Kern and Seto recently commented the concept of "Stimulating extracardiac collaterals" as follows: "To be clinically relevant, coronary collaterals should be a sustainable and sufficiently large source of myocardial perfusion and reduce ischemia in daily life. It is conceivable that improved extracardiac collateral flow has the potential to be exactly that."
This study is relevant due to its primary clinical in addition to surrogate marker efficacy testing, which has not been performed so far for this new technique of coronary arteriogenesis. If proven useful to extend physical exercise time in the context of mitigated angina pectoris, a further option of myocardial revascularization for patients with CAD not treatable by PCI or surgical bypass or not rendered asymptomatic by medical therapy would be available. The catheter-based technique of IMA device occlusion is simple and safe, and if shown efficacious, its action would be potentially sustainable due to the durability of occlusion.
Preclinical Evidence:
The efficacy to augment blood flow via the IMA as naturally existing extracardiac bypasses has been shown in experimental studies in dogs. Bilateral IMA ligation has led to an acute average increase in total coronary flow of about 6-10 ml/min.
The prevalent in vivo function of natural IMA-to-coronary artery bypasses and their anti-ischemic effect has been recently demonstrated during temporary IMA balloon occlusion by the investigators' research group. 180 pairs of measurements were performed in 120 patients electively referred for coronary angiography. Levels of collateral function and myocardial ischemia were determined during two coronary balloon occlusions, the first with, the second without distal IMA balloon occlusion.
Coronary collateral function, as determined by collateral flow index (CFI) has been consistently increased in the presence vs the absence of distal ipsilateral IMA balloon occlusion. These findings have been corroborated by the observed reduction in ischemia as assessed by intracoronary ECG (icECG). Conversely, with distal contralateral IMA occlusion, collateral function and ECG signs of ischemia have remained unchanged.
Clinical Evidence to Date:
Surgical trials in humans on the effect of bilateral IMA ligation on angina pectoris were carried out in the late 1950ies among a total of close to 500 symptomatic CAD patients. Transthoracic access to the IMAs was performed under local anesthesia by a small incision between the 2nd and 3rd rib. The primary endpoint of the clinical trials was angina pectoris, and inconsistently, ECG signs of myocardial ischemia. While the uncontrolled trials reported favourable results in terms of symptomatic relief of angina pectoris, the subsequently performed sham-controlled, but very small trials of bilateral ligation showed similar improvement in the sham as in the verum group. A major limitation of these studies lies in the rather insensitive endpoints used, which preclude conclusions about the efficacy of IMA ligation on extracardiac coronary collateral function.
In a prospective, open-label proof-of-concept trial, the investigators' laboratory occluded the right IMA (RIMA) permanently using a 4-5mm vascular plug in 50 CAD patients. As primary study endpoint, CFI was obtained during ostial, 1-minute balloon occlusion of the untreated right coronary artery (RCA) at baseline before RIMA device occlusion and 6 weeks later. CFI changed from 0.071±0.082 at baseline to 0.132±0.117 (p<0.0001) at follow-up examination. The increase in RCA CFI was accompanied by a decrease in signs of myocardial ischemia during the brief coronary occlusion.
The acute functional changes observed by the investigators' study group in response to temporary distal IMA balloon occlusion as well as the improvement of collateral function in the right coronary artery with permanent distal IMA occlusion support the hypothesis that extracardiac coronary collateral supply can be augmented by this intervention.
However, the effect of permanent IMA occlusion was never investigated with a randomized clinical trial. Consequently, our study group conducts a study, whereby 100 patients with chronic stable CAD (single-blinded for the procedure) are randomly allocated (1:1) to the occlusion or to a sham control group. The study endpoints (CFI and icECG and clinical signs of myocardial ischemia during RCA occlusion) as well as the follow-up duration of 6 weeks are identical in the current and the previous proof-of-concept trial
- Conditions
- Circulation, Collateral, Coronary Artery Disease, Internal Mammary-Coronary Artery Anastomosis, Ischemia
- Being tested
- Amplatzer vascular plug, Sham Controll
- Keywords
- Circulation, Collateral, Coronary Artery Disease, Internal Mammary-Coronary Artery Anastomosis, Ischemia
- Medical subject headings
- Coronary Artery Disease, Ischemia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Amplatzer vascular plugDevice
See above
Sham ControllOther
Angiography of the RIMA without occlusion
| Study group | Role | What they receive |
|---|---|---|
| Interventional Study Arm | Experimental | In the presence of a significant right coronary artery stenosis and randomization to the intervention group, 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, CE0086). Receives: Device: Amplatzer vascular plug |
| Sham-Control | Sham comparator | In the presence of a significant right coronary artery stenosis, and randomization to the sham-procedure: right IMA will be selectively intubated using an appropriate catheter. Angiography of the RIMA and the pericardiacophrenic branch will be performed. Receives: Other: Sham Controll |
What is being measured
The primary outcome is the main question the study is designed to answer.
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
Measured: Follow-up (week 6)
Secondary outcomes (4)
Angina pectoris
Occurence of Angina pectoris during a controlled 1-minute ostial coronary occlusion for collateral flow index measurement. The occurence will be presented in percent (number of patient with Angina pectoris during occlusion / total number of patients * 100 ) per group (intervention and sham control). If no adequate collateral flow exists, all patient (=100%) should develop angina pectoris during a one-minute occlusion.
Measured: Follow-up (week 6)
Change from baseline in intracoronary and surface ECG ST-segment shift during temporary right and left coronary balloon occlusion
Change from baseline in intracoronary and surface ECG ST-segment shift during temporary right and left coronary balloon occlusion at follow-up (week 6) vs baseline
Measured: Follow-up (week 6)
Fractional Flow Reserve
Change in coronary FFR (unitless) at follow-up (week 6) vs baseline.
Measured: Follow-up (week 6)
Number of patients with angiographic visibility of right IMA-to-coronary anastomoses
Angiographic visibility of right IMA-to-coronary anastomoses at follow-up
Measured: Follow-up (week 6)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 May 2019
- Study start8 Jul 2016
- Primary completion22 Feb 2019
- Study completion22 Feb 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (4)Papers the sponsor has linked to this study.
- Other trials for Circulation, CollateralStudies of the same condition, open and under way.
- More trials run by Insel Gruppe AG, University Hospital BernThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 100 participants (actual)
Sponsor and investigators
- Lead sponsor
- Insel Gruppe AG, University Hospital Bern
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Seiler Christian, MD, Prof, Principal investigator, Bern University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03950947
- Sponsor's protocol ID
- SNCTP000002493
- Acronym
- IMAOR
- Status last verified
- May 2019
- First submitted
- 13 May 2019
- Last updated
- 17 May 2019
- Results posted
- No
- Data monitoring committee
- Yes
- Individual data sharing
- Undecided
Publications
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.
PubMed 24744276Moberg 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.
PubMed 6025072BLAIR 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.
PubMed 13801236Bigler MR, Stoller M, Tschannen C, Grossenbacher R, Seiler C. Effect of permanent right internal mammary artery occlusion on right coronary artery supply: A randomized placebo-controlled clinical trial. Am Heart J. 2020 Dec;230:1-12. doi: 10.1016/j.ahj.2020.09.006. Epub 2020 Sep 17.
PubMed 32949505
Study at a glance
From the registry record, last updated by the sponsor on 17 May 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effect of Permanent Internal Mammary Artery Occlusion on Extracardiac Coronary Collateral Supply: a Randomized Controlled Study
- ClinicalTrials.gov ID
- NCT03950947
- Acronym / sponsor ID
- IMAOR / SNCTP000002493
- Conditions
- Circulation, Collateral, Coronary Artery Disease, Internal Mammary-Coronary Artery Anastomosis, Ischemia
- Keywords
- Circulation, Collateral, Coronary Artery Disease, Internal Mammary-Coronary Artery Anastomosis, Ischemia
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 100 participants (actual)
- Lead sponsor
- Insel Gruppe AG, University Hospital BernUniversity, hospital or other
- Study start
- 8 Jul 2016 (actual)
- Primary completion
- 22 Feb 2019 (actual)
- Study completion
- 22 Feb 2019 (actual)
- First posted
- 15 May 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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 internal mammary arteries (IMA)-to-coronary artery bypasses and their anti-ischemic effect has been recently demonstrated by the investigators' research group. Levels of collateral function and myocardial ischemia were determined in a prospective, open-label clinical trial of permanent IMA device occlusion. In this study, coronary collateral function, has been shown to be augmented in the presence vs the absence of distal permanent ipsilateral IMA occlusion. These findings have been corroborated by the observed reduction in ischemia in the intracoronary ECG.
After this first step, the concept of permanent right IMA occlusion will be now investigated with a randomized, sham-controlled clinical trial.
Detailed description
Despite considerable advances in medicine, cardiovascular diseases remain the number one cause of death globally. In industrialized countries, coronary artery disease (CAD) is the leading cause of death, consequence of myocardial infarction (MI).
In patients with acute coronary syndrome, percutaneous coronary intervention (PCI) has been shown to improve outcomes. For chronic stable CAD, a recent meta-analysis including more than 93'000 patients has concluded that there may be "evidence for improved survival with new generation drug eluting stents but no other percutaneous revascularization technology compared with medical treatment" . Conversely, a current review of recently published meta-analyses and the detailed analyses of 3 widely quoted individual studies indicate no difference exists among stable CAD patients between PCI and medical therapy regarding nonfatal myocardial infarct or all-cause or cardiovascular mortality. A very recently published randomized controlled trial among patients with stable, single-vessel CAD, the so called ORBITA trial, has found that PCI of the stenotic lesion did not prolong exercise time by more than the effect of a sham procedure during the short observation period of 6 weeks.
In contrast, coronary artery bypass grafting (CABG) was superior to PCI in patients with diabetes and multivessel CAD. CABG significantly reduced rates of death and myocardial infarction compared to PCI, but at a higher rate of stroke. Furthermore, in patients with advanced CAD, rates of myocardial infarction were more than 60% lower with CABG compared to PCI.
Conceptually, the benefit of CABG over PCI is not surprising as PCI targets significant coronary lesions thought to be responsible for causing ischemia. However, the deleterious effects of atherosclerosis are not typically preceded by significant luminal vascular narrowing. The vulnerable plaque eventually becoming the culprit plaque (causing myocardial infarction or sudden cardiac death) has typically a relatively mild stenosis. Furthermore, due to being multifocal and widespread, plaque vulnerability is not a target for, nor amenable to PCI.
Conversely, artificial - or natural - bypasses 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 (i.e. coronary arteriogenesis) as an alternative treatment strategy of revascularization to alter the course of CAD is attractive. In particular, promotion of natural coronary bypasses is an appealing concept for patients with CAD not or not entirely treatable by the conventional coronary revascularization methods of PCI and CABG. According to an analysis by Williams et al, 142 of 493 patients with chronic stable CAD (29%) belonged to the group with incomplete coronary revascularization (partial and no revascularization plus the so called no-option group), and this group showed reduced survival during the 3-year follow-up period. Coronary collateral function promotion from any source could, thus, contribute to the completeness of myocardial revascularization. Incomplete coronary revascularization in chronic CAD has been shown in a very large (n=35'993 patients), recently published registry-based study to reduce overall survival according to the number of vessels not treated by PCI and according to the severity of stenoses left untreated. Coronary arteriogenesis, i.e., the growth of pre-existing collateral vessels has to occur well in advance of acute atherothrombotic coronary artery occlusion in order to limit infarct size. The source of blood supply via natural coronary bypasses (collateral arteries) to a circulatory area at risk for infarction can be within the coronary circulation, but also via extracardiac paths, e.g., via internal mammary arteries (IMA; also termed internal thoracic arteries). Extracardiac coronary artery supply is conceptually related to the term coronary collateral circulation because of its known anatomical structure as arterial anastomoses between, e.g., IMA, the pericardium and coronary arterial branches. In an editorial, Kern and Seto recently commented the concept of "Stimulating extracardiac collaterals" as follows: "To be clinically relevant, coronary collaterals should be a sustainable and sufficiently large source of myocardial perfusion and reduce ischemia in daily life. It is conceivable that improved extracardiac collateral flow has the potential to be exactly that."
This study is relevant due to its primary clinical in addition to surrogate marker efficacy testing, which has not been performed so far for this new technique of coronary arteriogenesis. If proven useful to extend physical exercise time in the context of mitigated angina pectoris, a further option of myocardial revascularization for patients with CAD not treatable by PCI or surgical bypass or not rendered asymptomatic by medical therapy would be available. The catheter-based technique of IMA device occlusion is simple and safe, and if shown efficacious, its action would be potentially sustainable due to the durability of occlusion.
Preclinical Evidence:
The efficacy to augment blood flow via the IMA as naturally existing extracardiac bypasses has been shown in experimental studies in dogs. Bilateral IMA ligation has led to an acute average increase in total coronary flow of about 6-10 ml/min.
The prevalent in vivo function of natural IMA-to-coronary artery bypasses and their anti-ischemic effect has been recently demonstrated during temporary IMA balloon occlusion by the investigators' research group. 180 pairs of measurements were performed in 120 patients electively referred for coronary angiography. Levels of collateral function and myocardial ischemia were determined during two coronary balloon occlusions, the first with, the second without distal IMA balloon occlusion.
Coronary collateral function, as determined by collateral flow index (CFI) has been consistently increased in the presence vs the absence of distal ipsilateral IMA balloon occlusion. These findings have been corroborated by the observed reduction in ischemia as assessed by intracoronary ECG (icECG). Conversely, with distal contralateral IMA occlusion, collateral function and ECG signs of ischemia have remained unchanged.
Clinical Evidence to Date:
Surgical trials in humans on the effect of bilateral IMA ligation on angina pectoris were carried out in the late 1950ies among a total of close to 500 symptomatic CAD patients. Transthoracic access to the IMAs was performed under local anesthesia by a small incision between the 2nd and 3rd rib. The primary endpoint of the clinical trials was angina pectoris, and inconsistently, ECG signs of myocardial ischemia. While the uncontrolled trials reported favourable results in terms of symptomatic relief of angina pectoris, the subsequently performed sham-controlled, but very small trials of bilateral ligation showed similar improvement in the sham as in the verum group. A major limitation of these studies lies in the rather insensitive endpoints used, which preclude conclusions about the efficacy of IMA ligation on extracardiac coronary collateral function.
In a prospective, open-label proof-of-concept trial, the investigators' laboratory occluded the right IMA (RIMA) permanently using a 4-5mm vascular plug in 50 CAD patients. As primary study endpoint, CFI was obtained during ostial, 1-minute balloon occlusion of the untreated right coronary artery (RCA) at baseline before RIMA device occlusion and 6 weeks later. CFI changed from 0.071±0.082 at baseline to 0.132±0.117 (p<0.0001) at follow-up examination. The increase in RCA CFI was accompanied by a decrease in signs of myocardial ischemia during the brief coronary occlusion.
The acute functional changes observed by the investigators' study group in response to temporary distal IMA balloon occlusion as well as the improvement of collateral function in the right coronary artery with permanent distal IMA occlusion support the hypothesis that extracardiac coronary collateral supply can be augmented by this intervention.
However, the effect of permanent IMA occlusion was never investigated with a randomized clinical trial. Consequently, our study group conducts a study, whereby 100 patients with chronic stable CAD (single-blinded for the procedure) are randomly allocated (1:1) to the occlusion or to a sham control group. The study endpoints (CFI and icECG and clinical signs of myocardial ischemia during RCA occlusion) as well as the follow-up duration of 6 weeks are identical in the current and the previous proof-of-concept trial
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Interventional Study Arm | Experimental | Device: Amplatzer vascular plugIn the presence of a significant right coronary artery stenosis and randomization to the intervention group, 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, CE0086). |
| Sham-Control | Sham comparator | Other: Sham ControllIn the presence of a significant right coronary artery stenosis, and randomization to the sham-procedure: right IMA will be selectively intubated using an appropriate catheter. Angiography of the RIMA and the pericardiacophrenic branch will be performed. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- 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)
Key exclusion criteria (10 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Amplatzer vascular plugSee above | Device | Interventional Study Arm |
| Sham ControllAngiography of the RIMA without occlusion | Other | Sham-Control |
Primary outcome
Change from baseline in right coronary Collateral Flow Index (CFI)
Time frame: Follow-up (week 6)
Change from baseline in right coronary Collateral Flow Index (CFI) at follow-up (week 6) vs baseline
4 secondary outcomes
Angina pectoris
Time frame: Follow-up (week 6)
Change from baseline in intracoronary and surface ECG ST-segment shift during temporary right and left coronary balloon occlusion
Time frame: Follow-up (week 6)
Fractional Flow Reserve
Time frame: Follow-up (week 6)
Number of patients with angiographic visibility of right IMA-to-coronary anastomoses
Time frame: Follow-up (week 6)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 May 2019.
- Background: PubMed 24744276Stoller 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.
- Background: PubMed 6025072Moberg 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.
- Background: PubMed 13801236BLAIR 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.
- Derived from this study: PubMed 32949505Bigler MR, Stoller M, Tschannen C, Grossenbacher R, Seiler C. Effect of permanent right internal mammary artery occlusion on right coronary artery supply: A randomized placebo-controlled clinical trial. Am Heart J. 2020 Dec;230:1-12. doi: 10.1016/j.ahj.2020.09.006. Epub 2020 Sep 17.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Seiler Christian, MD, Prof principal investigator
Bern University Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Amplatzer vascular plug in people with Circulation, Collateral and Coronary Artery Disease, run by Insel Gruppe AG, University Hospital Bern at 1 site in Switzerland.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 17 May 2019. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change from baseline in right coronary Collateral Flow Index (CFI) (time frame: Follow-up (week 6)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03950947, which also lists 4 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 May 2019.