Trials / Completed
CompletedNCT00895427
A Study Comparing Skin Fluorescence to Coronary Artery Calcification
A Cross-Sectional Study Comparing Noninvasive Skin Fluorescence to Coronary Artery Calcification Measured by Rapid Computed Tomography
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 240 (estimated)
- Sponsor
- VeraLight, Inc. · Industry
- Sex
- All
- Age
- 45 Years
- Healthy volunteers
- Accepted
Summary
This study examines the relationship between the SCOUT DM device and coronary artery calcification as determined by rapid computed tomography in patients at risk for coronary heart disease.
Detailed description
This is a cross-sectional, single site, cohort screening trial. The correlation between the measured skin fluorescence and the CACS will be determined using a design that includes stratification by gender, subject age and subject CAC score. This design requires a single patient visit to the clinical site and a single measurement on the SCOUT device.
Conditions
Timeline
- Start date
- 2009-02-01
- Primary completion
- 2010-12-01
- Completion
- 2011-09-01
- First posted
- 2009-05-08
- Last updated
- 2011-10-12
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00895427. Inclusion in this directory is not an endorsement.