Status:
RECRUITING
Technical Development of Cardiovascular Magnetic Resonance Imaging (CMR) Using a Low Specific Absorption Rate (SAR) Scanner System
Lead Sponsor:
National Heart, Lung, and Blood Institute (NHLBI)
Conditions:
CAD
Eligibility:
All Genders
18-100 years
Phase:
NA
Brief Summary
Background: Researchers are testing version of a system known as a magnetic resonance imagining (MRI) scanner that uses strong magnetic fields, radio waves and the like to create images of the organs...
Detailed Description
Cardiac magnetic resonance imaging (CMR) provides accurate and reproducible measures of cardiac chamber volumes, cardiac function, blood flow, myocardial scar, myocardial extracellular volume as a mea...
Eligibility Criteria
Inclusion
- INCLUSION CRITERIA:
- Inclusion Criteria for All Participants (Objectives 1, 2, 3, and 4)
- Men and women age greater than or equal to 18 years
- Able to provide informed consent in writing
- Willingness to cooperate with all study procedures (including food restriction) and available for scheduled study events
- Inclusion Criteria for Healthy Volunteers (Objectives 1 and 2)
- Currently healthy, self-reported
- Inclusion Criteria for Subjects with Heart Disease (Objective 3)
- Subjects having known heart disease including but not limited to
- Stable angina pectoris due to epicardial coronary artery obstruction
- Past myocardial infarction
- Heart failure with reduced ejection fraction
- Valvular heart disease
- Pulmonary artery hypertension
- Congenital heart disease with or without prior repair
- Myocarditis
- Infiltrative cardiomyopathy
- Hypertrophic cardiomyopathy
- Inclusion Criteria for Subjects with Non-Cardiac Disease (Objective 4)
- Having known brain disease including but not limited to:
- Transient ischemic attack or stroke after 24 hours of onset
- Infection, inflammation meningitis
- Cognitive decline, neurodegenerative disorders
- Demyelinating disease, multiple sclerosis
- Loss of consciousness, seizures, epilepsy
- Brain tumor, metastases, abscess, lesion
- Vascular pathology
- Headache
- Hemorrhage
- Trauma
- Have known musculoskeletal disease including but not limited to:
- Persistent neck pain or radiculopathy
- Cancer or tumors of the spine
- Congenital abnormalities of the spinal cord or knee
- Multiple sclerosis
- Injury or trauma
- Fracture evaluation
- Infectious or inflammatory processes
- Soft tissue damage
- Muscle or tendon disorders
- Knee meniscal disorders
- Marrow abnormalities
- Mechanical knee symptoms
- Vascular conditions
- Have known abdominal diseases including but not limited to:
- Bowel obstruction
- Masses and tumors
- Crohns disease
- Diffuse liver disease such as hemochromatosis, hemosiderosis, fatty infiltration
- Focal hepatic lesions
- Cirrhotic liver
- Iron content determination
- Cystic kidney disease
- Vascular abnormalities
- Have known lung disease including but not limited to:
- Cancer, tumors and masses
- Vascular and lymphatic abnormalities
- Pulmonary thromboembolic disease
- Trauma
- Suspected bronchiolitis
- Bronchiectasis or pneumonitis
- Asthma and other obstructive lung diseases
- Pulmonary lymphangioleiomyomatosis
- Cystic and interstitial lung diseases such as pulmonary lymphangioleiomyomatosis and cystic fibrosis
- Have other known non-cardiovascular disease
- Inclusion criteria for bronchodilators:
- \- Only subjects who use bronchodilators routinely or those have undergone previous pulmonary function testing with bronchodilators will be invited to undergo bronchodilator testing during MRI.
- EXCLUSION CRITERIA:
- Exclusion Criteria for All Participants:
- Conditions that are thought to make MRI unsafe (that will be determined by filling out a separate form) including:
- Cerebral aneurysm clip unless it is labeled safe for MRI
- Neural stimulator (e.g. TENS-Unit) unless it is labeled safe for MRI
- Any type of ear implant unless it is labeled safe for MRI
- Ocular foreign body (e.g. metal shavings)
- Metal shrapnel or bullet
- Any implanted device (e.g. insulin pump, drug infusion device), unless it is labeled safe for MRI
- Pregnancy. When uncertain, subjects will undergo either urine or serum pregnancy testing. Results from up to 3 days prior to the examination will be used. Post-menopausal and surgically sterilized subjects are exempt from this testing.
- If a urine or serum pregnancy test was administered as part of a referral protocol, and the test was administered up to 3 days prior to MRI examination for this protocol, a new pregnancy test will not be required for this protocol.
- If a pregnancy test has not been administered within 3 days of MRI examination for this protocol, a serum or urine pregnancy test will be administered. Medical personnel will determine which pregnancy test is appropriate based on subject s medical history, screening, and individual scenario. In addition, the subject will be asked if she may be pregnant prior to the performance of the MRI, even if the pregnancy test was negative within the past week. The pregnancy test will be repeated if she answers in the affirmative.
- Exclusion Criteria for Gadolinium:
- When gadolinium based contrast agent (GBCA) exposure is planned
- Objective 1 and 2, Healthy Volunteers: No gadolinium based contrast agent exposure is permitted if eGFR \< 60 mL/min/1.73m\^(2) using the CKD-EPI equation or equivalent and a serum creatinine measured within 2 weeks without intercurrent change in medical condition or medications.
- Objective 3 and 4, Volunteers with Cardiac and Non-Cardiac Disease: No gadolinium based contrast agent exposure is permitted if eGFR \< 30 mL/min/1.73m\^(2) using the CKDEPI equation \[25\] or equivalent and a serum creatinine measured within 2 weeks without
- intercurrent change in medical condition or medications.
- -For all objectives not more than two research MRI exams with GBCA exposure in a 12 month period. Research MRI exams performed outside of this protocol will be included in the 12 month period.
- Subjects meeting this exclusion criterion, or without eGFR determination, may still be included in the study but may not be exposed to gadolinium-based contrast agents
- Breast feeding (unless subject is willing to discard breast milk for 24 hours)
- Does not wish to be exposed to gadolinium.
- Exclusion Criteria for Oxygen Inhalation:
- Severe chronic obstructive pulmonary disease defined as requiring more than one bronchodilator medication every day or continuous oxygen requiring
- Prior treatment with bleomycin
- Exclusion Criteria for Ferumoxytol Contrast
- A history of allergic reaction to any intravenous iron product
- Allergy to ferumoxytol or to mannitol excipient
- Breast feeding
- Does not wish to be exposed to ferumoxytol
- Iron overload
- Exclusion Criteria for oral contrast agent:
- A history of reaction to oral contrast (if using barium sulfate)
- Breast feeding unless subject is willing to discard breast milk for 24 hours (if using barium sulfate)
- Allergy to pineapple (if using pineapple juice)
- Does not wish to be exposed to oral contrast
- Exclusion Criteria for Healthy Volunteers (Objectives 1 and 2)
- Important past medical illness
- Exclusion Criteria for Adults with heart Disease (Objective 3)
- Unstable angina, acute coronary syndrome, or myocardial infarction not attributable to PCI, within 2 weeks unless after coronary revascularization of the culprit lesion.
- Any hemodynamic instability or decompensated heart failure as determined by the enrolling physician.
- Adenosine: Patients with asthma or chronic obstructive pulmonary disease of any severity are ineligible for vasodilator stress CMR with adenosine.
- Regadenoson: Only patients with severe or uncontrolled asthma or severe or uncontrolled chronic obstructive pulmonary disease are ineligible for vasodilator stress CMR with regadenoson. This will be determined at the discretion of the supervising provider based on medical records and physical exam.
- Patients with advanced heart block on baseline ECG are ineligible for vasodilator stress CMR
- Exclusion Criteria for Adults with Non-Cardiac Disease (Objective 4)
- Acute illness for which investigational imaging might delay care (such as acute stroke before treatment), as determined by the enrolling physician
- Any hemodynamic instability as determined by the enrolling physician.
- Exclusion criteria for bronchodilators:
- \- Patient refuses bronchodilator administration.
- Exclusion criteria for adults with cardiac implanted electronic devices (CIED, pacemakers or defibrillators:
- Low-SAR MRI:
- Subjects with MRI-conditional and legacy CIEDs are not excluded, based on the intrinsic safety of low-SAR MRI.
- Subjects with CIEDs are excluded if they have pacemakers implanted before 1998; ICDs implanted before 2000; temporary, epicardial or abandoned leads; and CIEDs implanted \<4 weeks prior to MRI exam.
- Conventional MRI:
- Subjects with CIED are excluded from conventional MRI unless they have CIEDs that are labeled as MRI conditional or MRI safe, and that are implanted greater than or equal to 4 weeks prior to MRI.
Exclusion
Key Trial Info
Start Date :
January 5 2018
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
May 31 2026
Estimated Enrollment :
2950 Patients enrolled
Trial Details
Trial ID
NCT03331380
Start Date
January 5 2018
End Date
May 31 2026
Last Update
December 4 2025
Active Locations (1)
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1
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892