Coronary Artery Disease Clinical Trial
Official title:
Prospective International Study of Coronary Subtraction Using 320 Row-Detector CT
| Verified date | August 13, 2018 |
| Source | National Institutes of Health Clinical Center (CC) |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
Background:
- This study is designed for people who need a standard, non-research invasive coronary
angiogram to find out if they have heart disease. Researchers want to take a computed
tomography (CT) scan of people s hearts before their procedure to see if this less invasive
test can also diagnose coronary artery disease.
Objectives:
- To learn if a new way to view CT pictures is able to accurately diagnose coronary artery
disease.
Eligibility:
- People age 55 and older who need a coronary angiogram.
Design:
- Participants will be screened with their medical records.
- Participants may give a blood sample.
- Participants may have a CT scan of the heart with and without contrast. The CT scan will
not interfere with their medical care.
- Participants blood pressure and heart rhythm will be monitored before, during, and after
the CT scan. They may have an electrocardiogram.
- Before the scan, participants will have an intravenous catheter put into their arm. It
will be used to inject contrast.
- Participants may take a beta blocker to slow their heart rate.
- Participants may take nitroglycerin under their tongue. It will enlarge their heart
blood vessels and improve picture quality. It may cause a flushing sensation or
headache.
- Participants will lie on their back on a padded table. The table slides into a large,
donut-shaped machine. An x-ray tube will move around their body, taking pictures. They
will be asked to hold their breath for 5 seconds at a time.
- Participants will be called 30 days after their angiogram. They will answer questions
about their health, hospital visits, or medical treatments.
| Status | Completed |
| Enrollment | 13 |
| Est. completion date | August 13, 2018 |
| Est. primary completion date | August 13, 2018 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 55 Years to 99 Years |
| Eligibility |
- INCLUSION CRITERIA: 1. Age over 55 years 2. Subjects referred for coronary angiography 3. Able to understand and willing to sign the Informed Consent Form EXCLUSION CRITERIA: 1. Known allergy to iodinated contrast media 2. Estimated GFR less than 50 ml/min 3. Atrial fibrillation or other continuous cardiac arrhythmias 4. Known or suspected intolerance or contraindication to beta-blocker medication (i.e. significant reactive airway disease, decompensated heart failure, Mobitz type 2 second degree or 3rd degree atrio-ventricular heart block) 5. Inability to adequately hold breath for 5 seconds 6. Pregnancy. Women of child bearing potential must demonstrate a negative pregnancy test within 24 hours of the study MDCT. |
| Country | Name | City | State |
|---|---|---|---|
| Denmark | Rigshospitalet | Copenhagen | |
| United States | National Institutes of Health Clinical Center, 9000 Rockville Pike | Bethesda | Maryland |
| Lead Sponsor | Collaborator |
|---|---|
| National Heart, Lung, and Blood Institute (NHLBI) |
United States, Denmark,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Coronary substraction CCTA improves the diagnostic accuracy. | 3 months |
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