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Validation of quantitative analysis method for myocardial blood flow using 3 Tesla myocardial perfusion MRI

Validation of quantitative analysis method for myocardial blood flow using 3 Tesla myocardial perfusion MRI - Quantitative analysis method of myocardial perfusion MRI

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000044612
Enrollment
70
Registered
2021-06-21
Start date
2021-07-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with known or suspected chronic coronary artery disease

Interventions

15O-H2O myocardial perfusion PET

Sponsors

Department of Radiology, Mie University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients with chronic coronary artery disease or suspected coronary artery disease who are referred for cardiac MRI following the clinical indication. (2) Adult patients aged 20 years or older at the time of MRI (3) Patients who have given written informed consent for participation in the study, including 15O-H2O myocardial perfusion PET.

Exclusion criteria

Exclusion criteria: 1) Patients with contraindications to the use of gadolinium contrast media 2) Patients with contraindications to ATP 3) Patients with severe claustrophobia 4) Patients with arrhythmias such as persistent atrial fibrillation or premature ventricular contraction 5) Patients who are unable to follow instructions to breath holding 6) Patients in an extremely poor general condition 7) Women who are pregnant or with suspected pregnancy 8) Patients with devices that are not MRI compatible 9) Patients with MRI-compatible devices (pacemakers, ICDs) that affect the quality of the MRI images 10) Patients who have had a cardiovascular event, revascularization procedure, change or addition of medication between cardiac MRI and myocardial perfusion PET. 11) Patients who are judged by the principal investigator or sub-investigator to be unsuitable for participation in the study.

Design outcomes

Primary

MeasureTime frame
In a pilot group, myocardial blood flow (MBF) determined by MRI will be compared with 15O-H2O PET to determine whether there are systematic errors in MBF. If a systematic error in MBF is found in the pilot group, a correction formula will be calculated and validated in a different group (validation group).

Secondary

MeasureTime frame
(1) Myocardial perfusion reserve (MPR) will be compared between quantitative myocardial perfusion MRI and 15O-H2O PET. (2) Diagnostic value of MBF and MPR determined by quantitative myocardial perfusion MRI will be investigated using coronary angiography, fractional flow reserve (FFR) and instantaneous wave-free ratio (iFR) as references, in patients undergoing coronary angiography.

Countries

Japan

Contacts

Public ContactMasaki Ishida

Mie University Hospital Department of Radiology

mishida@med.mie-u.ac.jp059-231-5029

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026