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Measuring heart muscle oxygenation in chest pain syndromes

Measuring Impairments in Myocardial Oxygenation in Chest Pain Syndrome Patients using Blood-level Dependent Magnetic Resonance Imaging

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12610000038099
Acronym
BOLD-MRI
Enrollment
65
Registered
2010-01-13
Start date
2010-02-01
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Interventions

Stress imaging with cardiac magnetic resonance (CMR)with half of the subjects receiving adenosine intravenously(140mcg/kg/min) for 3-6 mins once only during the CMR and the other half receiving dobutamine intravenously (maximal dose-40mcg/kg/min) once only during CMR, all subjects have an echocardiograph once only either before or after the CMR, for those subjects in the hibernating part of the study , (those patients who will have a revascularisation either coronary artery bypass graftingor per

Stress imaging with cardiac magnetic resonance (CMR)with half of the subjects receiving adenosine intravenously(140mcg/kg/min) for 3-6 mins once only during the CMR and the other half receiving dobutamine intravenously (maximal dose-40mcg/kg/min) once only during CMR, all subjects have an echocardiograph once only either before or after the CMR, for those subjects in the hibernating part of the study , (those patients who will have a revascularisation either coronary artery bypass graftingor percutaneous coronary intervention) only adenosine (140mcg/kg/min) for 3-6 mins will be used during the CMR. These subjects will have two CMR's one at baseline and then one six months post revascularisation.

Sponsors

Southern Adelaide Health Service
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Primary purpose
Diagnosis

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. History of hypertension, left ventricular hypertrophy, exertional chest pain and/or breathlessness, normal epicardial arteries 2. Known coronary artery disease, impaired regional left ventricular function awaiting percutaneous coronary intervention or coronary artery bypass grafting

Exclusion criteria

Inability to give written informed consent, estimated Glomerular Filtration Rate(GFR)<60mls/min, extreme claustrophobia, implantable cardiac devices and other contra-indications to Magnetic Resonance Imaging(MRI) (i.e. metal in eyes), asthma or other reversible bronchospasm

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026