Utility of Regadenoson Low-dose Dynamic Computed Tomography for Myocardial Perfusion Assesment (ULYSSES Study).

National Institute of Cardiology, Warsaw, Poland

Status: Completed

Conditions: Coronary Artery Disease; Computed Tomography; Myocardial Perfusion Imaging

Study type: Observational

Funder types: Other

Identifiers

NCT03917199

2015/19/B/NZ5/03502

Details and patient eligibility

About

The ULYSSES study is a single-center, prospective study aimed at evaluation of myocardial ischemia using regadenoson low-dose dynamic computed tomography myocardial perfusion imaging (CTP) in patients diagnosed with intermediate coronary artery stenoses in referrence to the magnetic resonance myocardial perfusion imaging (MR MPI).

Full description

The ULYSSES study is a single-center, prospective study aimed at evaluation of myocardial ischemia using regadenoson low-dose dynamic computed tomography myocardial perfusion (CTP) in patients diagnosed with intermediate coronary artery stenoses in referrence to the magnetic resonance myocardial perfusion imaging (MR MPI).

The main objectives of the study are:

• to evaluate feasibility of low - dose regadenoson dynamic computed tomography myocardial imaging protocol
• to assess the diagnostic value of quantitative dynamic CTP based absolute parameters (myocardial blood flow - MBF, myocardial blood volume - MBV, perfused capillary blood volume - PCBV, peak value - PV, time to peak - TTP) in reference to magnetic resonance myocardial perfusion imaging
• to assess the diagnostic value of quantitative dynamic CTP based relative parameters (relative myocardial blood flow - MBFR, relative myocardial blood volume - MBVR, relative perfused capillary blood volume - PCBVR, relative peak value - PVR, relative time to peak - TTPR) in reference to magnetic resonance myocardial perfusion imaging
• evaluation of safety of regadenoson low-dose dynamic CTP.

Enrollment: 60 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• age over 18 years
• signing written, informed consent by the patient for participation in the study
• patients who are asymptomatic or with symptoms of stable coronary heart disease
• intermediate coronary artery stenosis of at least one coronary artery in CTCA

Exclusion criteria

• the symptoms of unstable ischemic heart disease and /or myocardial infarction,
• the history of myocardial infarction
• patients with impaired renal function (GFR <60 mL)
• contraindications for computed tomography or magnetic resonance imaging (including pregnancy, the presence of a cardiac pacemaker or cardioverter-defibrillator, claustrophobia, the presence of metal elements, etc.);
• contraindications to the administration of iodine contrast media (including allergy to contrast, unstable hyperthyroidism, etc.)
• contraindications to administration of regadenosone (hypersensitivity to the active substance, second or third degree atrioventricular block or other sinus node dysfunction, unstable angina, hypotension, decompensated heart failure, etc.);
• heart failure with impaired left ventricular systolic function
• a significant valvular heart disease
• presence of aortic aneurysm or aortic dissection
• persistent atrial fibrillation / atrial flutter
• hypertrophic cardiomyopathy