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Detection of Subclinical Atherosclerosis in Asymptomatic Individuals

Prospective Detection of Subclinical Atherosclerosis in Asymptomatic Individuals With High Likelihood of Coronary Artery Disease With a Novel, Low-Radiation Volumetric Computed Tomography Approach

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00862056
Acronym
Decide CTA
Enrollment
73
Registered
2009-03-16
Start date
2009-01-31
Completion date
2013-07-31
Last updated
2017-11-20

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

Conditions

Coronary Artery Disease

Keywords

asymptomatic, coronary artery disease

Brief summary

This study will evaluate the use of cardiac CT in identifying atherosclerosis plaque in patients who have not been diagnosed with atherosclerosis and who have no symptoms of the disease but who are at risk of developing atherosclerosis based on traditional risk factors such as diabetes or a family history of coronary artery disease.

Interventions

PROCEDURECardiac CT

All participants will undergo a coronary artery CT angiogram with contrast.

Sponsors

Piedmont Healthcare
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
35 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* Males between ages 35-90 or females between ages 40-90 * No known coronary artery disease * no prior coronary disease by cardiac catheterization (no more than 40% in any major epicardial vessel) * no prior myocardial infarction * no prior ST-elevation myocardial infarction (1 mm ST-elevation in 2 contiguous leads) * no prior non-ST-elevation myocardial infarction (CK-MB \> 2x ULN or elevated troponin that is indicative of myocardial necrosis based on local institutional cutpoints) * no prior coronary revascularization procedure * Aymptomatic * no chest pain, shortness of breath, angina or angina-equivalent that is assumed to be related to myocardial ischemia * Presence of a high-risk feature (at least one of the following four will quality) * High FRS ≥20% (http://hp2010.nhlbihin.net/atpiii/calculator.asp) * Diabetes Mellitus * Premature CAD in a first-degree relative * High Risk Lipid Profile (must meet one of the following laboratory criteria) 1. LDL \> 250 mg/dL 2. HDL \< 20 mg/dL 3. Triglycerides \> 1000 mg/dL 4. LP(a) \> 80 mg/dL * Provide written informed consent and Authorization for Use/Disclosure of PHI

Exclusion criteria

* Known genetic form of hypercholesterolemia based on clinical criteria (e.g. familial hypercholesterolemia, etc.) * Creatinine 1.5 mg/dL or greater * Irregular rhythm precluding cardiac CT examination * Uncontrolled hypertension (SBP\>210 mmHg or DBP\>140 mmHg on treatment) * Known moderate or severe allergy to iodine-based contrast agents (mild prior reactions that could be treated as an outpatient or that could be prevented by pre-medication in the past do not constitute exclusion) * Known Pregnancy * Unwilling or unable to consent * Presence of any co-morbidity that makes life expectancy less than 24 months * Unwilling or unable to complete follow-up * Unwilling or unable to provide written informed consent and Authorization for Use/Disclosure of PHI

Design outcomes

Primary

MeasureTime frame
The primary endpoint of the study is identifying the prevalence of coronary artery disease (CAD) in an asymptomatic population of patients without prior history of, but with high likelihood of CAD.6 months, 1 year

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026