Registry for CARDIAC PERFUSION CT

Withdrawn before enrolling

Conditions studied: Coronary Artery Disease

In brief

This protocol describes a study whose goal is to collect de-identified Cardiac CT Perfusion (CTP) acquisition parameters and clinical findings from approximately 20 qualified medical facilities. The study uses an electronic data capture tool to collect the de-identified data to create a global multi-center registry. This registry will be used for scientific analysis and publication of pertinent medical trends such as CT utilization, radiation dose, and common cardiovascular findings.

Key facts

Study ID

NCT01346605

Run by

MDDX LLC

People needed

0

Starts

2011-05-01

Expected to finish

2012-08-01

Last updated by the study team

2012-12-11

Who can join

Age: 35 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Moderate-high likelihood of coronary artery disease with a prior stress SPECTMPI exam likely to be referred to the cardiac catheterization laboratory for invasive angiogram or patients presenting with clinical indication of Coronary -CT Angiography and an initial calcium score above 300
• Stable angina or anginal equivalent as the chief symptom.
• Age > 34 years old
• Able to comprehend and sign the consent form.

You may not qualify if…

• BMI<41
• Acute coronary syndromes (unstable angina, non-ST elevation myocardial infarction, ST elevation myocardial infarction)
• Unstable clinical conditions (i.e. hemodynamic instability, arrhythmias)
• Premenopausal women who have menstruated in the last year
• Glomerular Filtration Rate (GFR) < 60 ml/min/BSA as an indicator of renal insufficiency
• Known allergy to iodinated contrast agents
• Patients who are on metformin medication for any reason
• Atrial fibrillation
• Asthma
• Critical aortic stenosis
• Systolic blood pressure < 90 mmHg
• Advanced heart block
• Pacemaker or AICD

Where it is running

• Miami Baptist — Miami, Florida, United States

Full record on ClinicalTrials.gov

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