Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 5:00 PM
Ignite Modification Date:
2025-12-24 @ 5:00 PM
NCT ID:
NCT01816750
Eligibility Criteria:
Inclusion Criteria:
Accuracy arm
* Patients \>50 years of age
* Suspected or known coronary artery disease referred for ICA
Stress perfusion arm
* Patients \>50 years of age
* Suspected or established coronary artery disease referred for MPI-SPECT for assessment of inducible ischaemia
Delayed enhancement arm
* Patients \>50 years of age
* Referred for CMR for assessment of myocardial viability/scar
Exclusion Criteria:
Accuracy arm
* Consent cannot be obtained
* Patient BMI \> 30 kg /m2
* NYHA class III or IV heart failure
* Chronic total occlusion of target epicardial coronary artery
* Urgent revascularisation required
* Allergy to iodinated contrast or previous contrast induced nephropathy
* Intolerance or contraindication to beta-blockers
* Uncontrolled heart rhythm disturbances
* 2nd or 3rd degree atrioventricular block
* Estimated glomerular filtration rate \<30ml/min within two weeks prior to procedure or chronic renal failure on dialysis
* Pregnancy
Stress perfusion arm
* As above, plus:
* Asthma (any) or intolerance to adenosine
Delayed enhancement arm
\- As for Accuracy arm
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
50 Years
Study:
NCT01816750
Study Brief:
Protocol Section:
NCT01816750