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Predictor of Advanced Sub-Clinical Atherosclerosis (PASA) Study

Predictor of Advanced Sub-Clinical Atherosclerosis (PASA) Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00258999
Enrollment
600
Registered
2005-11-28
Start date
2005-10-31
Completion date
2007-11-30
Last updated
2015-10-05

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

Conditions

Atherosclerosis

Keywords

Skin Cholesterol, Carotid Plaque, Carotid Intima-Media Thickness

Brief summary

The study will evaluate the clinical utilization of skin Cholesterol (SC) for cardiovascular risk assessment in asymptomatic individuals at low, intermediate and high risk based on Framingham global risk estimates. Preliminary studies have suggested that SC is an easy to measure, noninvasive marker of cardiovascular risk. This study is intended to provide further data in support of broader clearance by the Food and Drug Administration for the use of SC as a tool to identify asymptomatic patients at increased risk of cardiovascular disease. Currently, SC testing is cleared for use as part of risk assessment in subject suspected of having significant multi-vessel disease. The current study data will be used to support the use of SC testing as part of cardiovascular risk assessment in subjects without suspected coronary artery disease (CAD).

Detailed description

* The primary objective of the study will be to determine the relationship between skin cholesterol levels and carotid artery intima-media thickness (CIMT), a surrogate marker for atherosclerotic burden used as the gold standard comparator. * Secondary objectives of the study will be to compare the skin cholesterol levels with other markers of CAD as HDL cholesterol, Apo B, hsCRP, and lipoprotein-association phospholipase A2. * Another objective is to determine the relationship between skin cholesterol levels and the presence of carotid plaques detected by ultrasound.

Interventions

DEVICESkin Cholesterol Testing

Sponsors

University of Wisconsin, Madison
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Informed written consent from the subject prior to testing. * Males or females 30-80 years of age

Exclusion criteria

* 1\. Known coronary heart disease, (history of myocardial infarction, coronary bypass surgery, coronary angioplasty, or angina pectoris with a positive stress test or angiographic documentation) * Known peripheral vascular disease (claudication with ankle-brachial index \< 0.9, angioplasty, or peripheral artery bypass procedure) * Known cerebrovascular disease (stroke or TIA with documented carotid or aortic atherosclerosis) * History of carotid artery endarterectomy or carotid artery surgery * Diabetes mellitus (fasting glucose \> 126 mg/dL, on on insulin-reducing medications) * 10-year Framingham risk of cardiac death or MI using ATP III calculator \>20% * Subjects taking cholesterol-lowering medications * Known hepatitis * Known pregnancy * Skin disease on either hand (e.g. eczema psoriasis, rash or broken skin)

Design outcomes

Primary

MeasureTime frame
The primary analysis will test if SC is a predictor of elevated CIMT (i.e. carotid wall thickness above the 75% percentile expected for subject's age sex and race based on projections from the Atherosclerosis Risk in Communities Study)

Secondary

MeasureTime frame
Secondarily, estimates of relative risk will allow the comparison of the power of SC as a predictor and traditional risk and new emerging risk factors(hsCRP, Apo B100 and Phospholipase A2).

Countries

United States

Outcome results

None listed

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