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CArdiac magnetic resonance perfusioN imaging for SELection of patients for additional invasive evaluation after CT coronary angiography (CANSEL)

CArdiac magnetic resonance perfusioN imaging for SELection of patients for additional invasive evaluation after CT coronary angiography (CANSEL) - CANSEL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON31103
Enrollment
75
Registered
2007-08-06
Start date
2007-08-20
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

coronary atherosclerosis MRI

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Suspected obstructive CAD on CT-CA 2. Planned invasive coronary angiography

Exclusion criteria

Exclusion criteria: 1. Previous myocardial infarction 2. Previous percutaneous coronary intervention or coronary artery bypass grafting 3. Contraindications for MRI 4. Possible pregnancy and/or breast feeding 5. Inability to breath hold for up to 15 seconds 6. Inability to give reliable informed consent 7. Known claustrophobia 8. Unstable coronary artery disease 9. Known allergy to contrast material 10. Renal insufficiency 11. COPD.

Design outcomes

Primary

MeasureTime frame
We expect a high sensitivity and specificity for first pass magnetic resonance imaging to detect a significant coronary artery stenosis as determined by FFR. Determination optimal cut of value. There is no benefit for the individual patient. In the future in patients with coronary stenosis identified by CT-CA, myocardial perfusion MRI will predict who may benefit from coronary revascularisation. Furthermore the combination of CT-CA, and myocardial perfusion study using magnetic resonance will also predict who do not have a coronary stenosis and therefore do not need ICA.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)