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Early Detection of Silent Myocardial Ischemia (EarlySynergy)

Primary Purpose

Ischemic Heart Disease, Silent Myocardial Ischemia, Cardiovascular Diseases

Status
Enrolling by invitation
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
CMR stress perfusion imaging
Sponsored by
Pim van der Harst
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Ischemic Heart Disease

Eligibility Criteria

45 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Participation in ROBINSCA or ImaLife study
  • CT-CAC ≥300

Exclusion Criteria:

  • History of ischemic heart disease or other cardiac disease (myocardial infarction, sudden cardiac arrest, heart failure, cardiomyopathy, congenital cardiac disease, percutaneous coronary intervention, coronary artery bypass grafting surgery, valvular surgery, other major cardiac surgery (e.g. cardiac transplantation) and/or previous invasive coronary angiography or catheter ablation)
  • Contra-indication for stress CMR perfusion imaging (claustrophobia, CMR incompatible device (e.g., Implantable Cardioverter Defibrillator/pacemaker), contrast agent or vasodilator intolerance, contra-indications for adenosine or regadenoson (e.g. 2nd/3rd degree atrioventricular block, severe hypotension) and/or weight > 125 kg)
  • Severe comorbidity and/or a life expectancy of less than 1 year
  • Unable to provide written informed consent
  • Pregnancy

Sites / Locations

  • University Medical Center Groningen

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Cardiac magnetic resonance imaging

Control

Arm Description

Cardiac magnetic resonance (CMR) stress perfusion imaging with feedback of clinically actionable findings

No intervention, following the natural course of coronary atherosclerosis

Outcomes

Primary Outcome Measures

Rate of major adverse cardiac events
Cardiovascular death, non-fatal myocardial infarction or hospitalization for unstable angina, heart failure or resuscitated cardiac arrest
Rate of major adverse cardiac events
Cardiovascular death, non-fatal myocardial infarction or hospitalization for unstable angina, heart failure or resuscitated cardiac arrest
Rate of major adverse cardiac events
Cardiovascular death, non-fatal myocardial infarction or hospitalization for unstable angina, heart failure or resuscitated cardiac arrest
Diagnostic yield of CMR stress perfusion imaging
Prevalence and extent of silent myocardial ischemia and cardiac dysfunction

Secondary Outcome Measures

Rate of individual components of primary outcome 1
Cardiovascular death, non-fatal myocardial infarction or hospitalization for unstable angina, heart failure or resuscitated cardiac arrest
Rate of individual components of primary outcome 1
Cardiovascular death, non-fatal myocardial infarction or hospitalization for unstable angina, heart failure or resuscitated cardiac arrest
Rate of individual components of primary outcome 1
Cardiovascular death, non-fatal myocardial infarction or hospitalization for unstable angina, heart failure or resuscitated cardiac arrest
All-cause mortality rate
Death from any disease
All-cause mortality rate
Death from any disease
All-cause mortality rate
Death from any disease
Rate of invasive cardiovascular procedures
percutaneous coronary intervention (PCI), coronary artery bypass grafting (CABG) surgery, invasive coronary angiography (ICA) and other invasive cardiovascular procedures
Rate of invasive cardiovascular procedures
percutaneous coronary intervention (PCI), coronary artery bypass grafting (CABG) surgery, invasive coronary angiography (ICA) and other invasive cardiovascular procedures
Rate of invasive cardiovascular procedures
percutaneous coronary intervention (PCI), coronary artery bypass grafting (CABG) surgery, invasive coronary angiography (ICA) and other invasive cardiovascular procedures
Rate of hospitalization for cardiovascular disease
Hospitalization for cardiovascular disease (e.g. stroke, peripheral vascular disease)
Rate of hospitalization for cardiovascular disease
Hospitalization for cardiovascular disease (e.g. stroke, peripheral vascular disease)
Rate of hospitalization for cardiovascular disease
Hospitalization for cardiovascular disease (e.g. stroke, peripheral vascular disease)
Rate of non-invasive cardiac imaging procedures
Rate of non-invasive cardiac imaging procedures (e.g., myocardial stress perfusion imaing, echocardiography)
Rate of medical therapy initiation
Initiation of preventive or cardio-active medication (e.g., ACE-inhibiters, statins, calcium antagonists, beta-blockers etc.)
Rate of medical therapy initiation
Initiation of preventive or cardio-active medication (e.g., ACE-inhibiters, statins, calcium antagonists, beta-blockers etc.)
Rate of medical therapy initiation
Initiation of preventive or cardio-active medication (e.g., ACE-inhibiters, statins, calcium antagonists, beta-blockers etc.)
Quality of Life as reflected by EQ-5D-5S score
Quality of life as assessed by EQ-5D-5S questionnaire
Quality of Life as reflected by EQ-5D-5S score
Quality of life as assessed by EQ-5D-5S questionnaire
Quality of Life as reflected by EQ-5D-5S score
Quality of life as assessed by EQ-5D-5S questionnaire
Quality of Life as reflected by HeartQoL score
Quality of life as assessed by HeartQoL questionnaire
Quality of Life as reflected by HeartQoL score
Quality of life as assessed by HeartQoL questionnaire
Quality of Life as reflected by HeartQoL score
Quality of life as assessed by HeartQoL questionnaire

Full Information

First Posted
December 11, 2020
Last Updated
April 29, 2021
Sponsor
Pim van der Harst
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1. Study Identification

Unique Protocol Identification Number
NCT04680338
Brief Title
Early Detection of Silent Myocardial Ischemia
Acronym
EarlySynergy
Official Title
Early Detection of Silent Myocardial Ischemia and Cardiac Dysfunction in Asymptomatic Individuals With Increased Coronary Artery Calcium Scores
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Enrolling by invitation
Study Start Date
May 27, 2019 (Actual)
Primary Completion Date
December 2021 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Pim van der Harst

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
Early-Synergy investigates a diagnostic imaging approach in asymptomatic individuals from the general population for early detection of silent myocardial ischemia and cardiac dysfunction. The diagnostic imaging approach consists of cardiac computed tomography for coronary artery calcium scoring (CT-CAC) and cardiac magnetic resonance (CMR) stress perfusion imaging. Early-Synergy investigates the effect of early detection of silent myocardial ischemia and cardiac dysfunction by CMR in asymptomatic individuals with increased CAC. In addition, the diagnostic yield of CMR for early detection of silent myocardial ischemia and cardiac dysfunction is investigated. Asymptomatic individuals at increased risk (CAC ≥ 300) are therefore randomized 1:1 to either CMR stress perfusion imaging or a control group.
Detailed Description
Early-Synergy is a prospective multi-center study performed in the Netherlands. Potential candidates for participation in Early-Synergy have had CT-CAC scanning as part of participation in two ongoing population-based studies (ROBINSCA and ImaLife) and had CAC ≥300. Participants are randomized in a 1:1 fashion to (1.) CMR stress perfusion imaging with feedback of clinically actionable findings or (2.) control group. In the CMR group, feedback on CMR stress perfusion imaging is provided to the participant and general practitioner only in case of CMR findings that require further management based on current clinical guidelines. Participants in the control group will not receive stress CMR perfusion imaging but will be followed in time to evaluate the clinical presentation of the natural course of coronary atherosclerosis. Follow-up will be performed up to 5 years in both groups by sending questionnaires and collecting medical information from health care providers and registries. Additionally, blood is drawn from participants in the CMR group during the hospital visit for CMR scanning and is stored to allow evaluation of cardiac blood markers as predictors of CMR findings.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemic Heart Disease, Silent Myocardial Ischemia, Cardiovascular Diseases

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1400 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cardiac magnetic resonance imaging
Arm Type
Active Comparator
Arm Description
Cardiac magnetic resonance (CMR) stress perfusion imaging with feedback of clinically actionable findings
Arm Title
Control
Arm Type
No Intervention
Arm Description
No intervention, following the natural course of coronary atherosclerosis
Intervention Type
Diagnostic Test
Intervention Name(s)
CMR stress perfusion imaging
Intervention Description
CMR stress perfusion imaging with feedback of clinically actionable findings to general practitioner and participant
Primary Outcome Measure Information:
Title
Rate of major adverse cardiac events
Description
Cardiovascular death, non-fatal myocardial infarction or hospitalization for unstable angina, heart failure or resuscitated cardiac arrest
Time Frame
1 year
Title
Rate of major adverse cardiac events
Description
Cardiovascular death, non-fatal myocardial infarction or hospitalization for unstable angina, heart failure or resuscitated cardiac arrest
Time Frame
2.5 years
Title
Rate of major adverse cardiac events
Description
Cardiovascular death, non-fatal myocardial infarction or hospitalization for unstable angina, heart failure or resuscitated cardiac arrest
Time Frame
5 years
Title
Diagnostic yield of CMR stress perfusion imaging
Description
Prevalence and extent of silent myocardial ischemia and cardiac dysfunction
Time Frame
Baseline
Secondary Outcome Measure Information:
Title
Rate of individual components of primary outcome 1
Description
Cardiovascular death, non-fatal myocardial infarction or hospitalization for unstable angina, heart failure or resuscitated cardiac arrest
Time Frame
1 year
Title
Rate of individual components of primary outcome 1
Description
Cardiovascular death, non-fatal myocardial infarction or hospitalization for unstable angina, heart failure or resuscitated cardiac arrest
Time Frame
2.5 years
Title
Rate of individual components of primary outcome 1
Description
Cardiovascular death, non-fatal myocardial infarction or hospitalization for unstable angina, heart failure or resuscitated cardiac arrest
Time Frame
5 years
Title
All-cause mortality rate
Description
Death from any disease
Time Frame
1 year
Title
All-cause mortality rate
Description
Death from any disease
Time Frame
2.5 years
Title
All-cause mortality rate
Description
Death from any disease
Time Frame
5 years
Title
Rate of invasive cardiovascular procedures
Description
percutaneous coronary intervention (PCI), coronary artery bypass grafting (CABG) surgery, invasive coronary angiography (ICA) and other invasive cardiovascular procedures
Time Frame
1 year
Title
Rate of invasive cardiovascular procedures
Description
percutaneous coronary intervention (PCI), coronary artery bypass grafting (CABG) surgery, invasive coronary angiography (ICA) and other invasive cardiovascular procedures
Time Frame
2.5 years
Title
Rate of invasive cardiovascular procedures
Description
percutaneous coronary intervention (PCI), coronary artery bypass grafting (CABG) surgery, invasive coronary angiography (ICA) and other invasive cardiovascular procedures
Time Frame
5 years
Title
Rate of hospitalization for cardiovascular disease
Description
Hospitalization for cardiovascular disease (e.g. stroke, peripheral vascular disease)
Time Frame
1, 2.5, 5 years
Title
Rate of hospitalization for cardiovascular disease
Description
Hospitalization for cardiovascular disease (e.g. stroke, peripheral vascular disease)
Time Frame
1 year
Title
Rate of hospitalization for cardiovascular disease
Description
Hospitalization for cardiovascular disease (e.g. stroke, peripheral vascular disease)
Time Frame
2.5 years
Title
Rate of non-invasive cardiac imaging procedures
Description
Rate of non-invasive cardiac imaging procedures (e.g., myocardial stress perfusion imaing, echocardiography)
Time Frame
5 years
Title
Rate of medical therapy initiation
Description
Initiation of preventive or cardio-active medication (e.g., ACE-inhibiters, statins, calcium antagonists, beta-blockers etc.)
Time Frame
1 year
Title
Rate of medical therapy initiation
Description
Initiation of preventive or cardio-active medication (e.g., ACE-inhibiters, statins, calcium antagonists, beta-blockers etc.)
Time Frame
2.5 years
Title
Rate of medical therapy initiation
Description
Initiation of preventive or cardio-active medication (e.g., ACE-inhibiters, statins, calcium antagonists, beta-blockers etc.)
Time Frame
5 years
Title
Quality of Life as reflected by EQ-5D-5S score
Description
Quality of life as assessed by EQ-5D-5S questionnaire
Time Frame
1 year
Title
Quality of Life as reflected by EQ-5D-5S score
Description
Quality of life as assessed by EQ-5D-5S questionnaire
Time Frame
2.5 years
Title
Quality of Life as reflected by EQ-5D-5S score
Description
Quality of life as assessed by EQ-5D-5S questionnaire
Time Frame
5 years
Title
Quality of Life as reflected by HeartQoL score
Description
Quality of life as assessed by HeartQoL questionnaire
Time Frame
1 year
Title
Quality of Life as reflected by HeartQoL score
Description
Quality of life as assessed by HeartQoL questionnaire
Time Frame
2.5 years
Title
Quality of Life as reflected by HeartQoL score
Description
Quality of life as assessed by HeartQoL questionnaire
Time Frame
5 years
Other Pre-specified Outcome Measures:
Title
Cost-effectiveness
Description
Cost-effectiveness of CMR stress perfusion imaging compared to control group
Time Frame
1 year
Title
Cost-effectiveness
Description
Cost-effectiveness of CMR stress perfusion imaging compared to control group
Time Frame
2.5 years
Title
Cost-effectiveness
Description
Cost-effectiveness of CMR stress perfusion imaging compared to control group
Time Frame
5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Participation in ROBINSCA or ImaLife study CT-CAC ≥300 Exclusion Criteria: History of ischemic heart disease or other cardiac disease (myocardial infarction, sudden cardiac arrest, heart failure, cardiomyopathy, congenital cardiac disease, percutaneous coronary intervention, coronary artery bypass grafting surgery, valvular surgery, other major cardiac surgery (e.g. cardiac transplantation) and/or previous invasive coronary angiography or catheter ablation) Contra-indication for stress CMR perfusion imaging (claustrophobia, CMR incompatible device (e.g., Implantable Cardioverter Defibrillator/pacemaker), contrast agent or vasodilator intolerance, contra-indications for adenosine or regadenoson (e.g. 2nd/3rd degree atrioventricular block, severe hypotension) and/or weight > 125 kg) Severe comorbidity and/or a life expectancy of less than 1 year Unable to provide written informed consent Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pim van der Harst, MD, PhD
Organizational Affiliation
University Medical Center Groningen
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Medical Center Groningen
City
Groningen
ZIP/Postal Code
9713 GZ
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data management plan in progress
IPD Sharing Time Frame
In accordance with legal period for study data storage
IPD Sharing Access Criteria
In correspondence with the principal investigator
Citations:
PubMed Identifier
31016436
Citation
Xia C, Rook M, Pelgrim GJ, Sidorenkov G, Wisselink HJ, van Bolhuis JN, van Ooijen PMA, Guo J, Oudkerk M, Groen H, van den Berge M, van der Harst P, Dijkstra H, Vonder M, Heuvelmans MA, Dorrius MD, De Deyn PP, de Bock GH, Dotinga A, Vliegenthart R. Early imaging biomarkers of lung cancer, COPD and coronary artery disease in the general population: rationale and design of the ImaLife (Imaging in Lifelines) Study. Eur J Epidemiol. 2020 Jan;35(1):75-86. doi: 10.1007/s10654-019-00519-0. Epub 2019 Apr 23.
Results Reference
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PubMed Identifier
28843465
Citation
Vonder M, van der Aalst CM, Vliegenthart R, van Ooijen PMA, Kuijpers D, Gratama JW, de Koning HJ, Oudkerk M. Coronary Artery Calcium Imaging in the ROBINSCA Trial: Rationale, Design, and Technical Background. Acad Radiol. 2018 Jan;25(1):118-128. doi: 10.1016/j.acra.2017.07.010. Epub 2017 Aug 23.
Results Reference
background

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Early Detection of Silent Myocardial Ischemia

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