Phase
Condition
Chest Pain
Heart Failure
Congestive Heart Failure
Treatment
N/AClinical Study ID
Ages > 18 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
All participants will be over the age of 18 and able to provide consent
Group A (volunteers, with or without cardiac disease): Volunteers will beavailable for at least one study visit
Group B (HFpEF patient volunteers): Volunteers will have a diagnosis of HFpEF andbe safe to be imaged with MRI
Exclusion
Exclusion Criteria:
minors
Critically ill patients, patients on ventilators, patients with unstable angina orwith hypotension, asthmatics, and other patients whose medical care or safety may beat risk from undergoing an MRI examination will be excluded.
Patients with claustrophobia will also be excluded from the study if this cannot becontrolled with standard methods (valium or benadryl).
Patients with contraindication to MRI (metal implants, or certain types of heartvalves),
pregnant patients, , mentally disabled patients and prisoners will be excluded fromthis study. (All criteria apply to patients and normal volunteers).
Gadolinium nephrotoxicity will be addressed by having patients with abnormal kidneyfunction (GFR<30) excluded from the study due to the (very small) risk associated withgadolinium contrast agents.
This threshold may be modified, depending on practices determined by the RadiologyDepartment and the IRB.
Patients with a known allergy or contraindication to Adenosine and/or Regadenoson willbe excluded from stress MRI cohorts.
All participants that will receive a stress agent will refrain from consuming caffeinefor at least 12 hours prior to each MRI
Subjects with a known contraindication to Adenosine and/or Regadenoson will only beenrolled in scans where no stress agent will be administered
Study Design
Study Description
Connect with a study center
university of Utah, Radiology Research
Salt Lake City, Utah 84108
United StatesActive - Recruiting
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