NCT00895427已完成不适用
A Cross-Sectional Study Comparing Noninvasive Skin Fluorescence to Coronary Artery Calcification Measured by Rapid Computed Tomography
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 240
- 试验地点
- 1
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 45 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Males ≥ 45 years or females ≥ 50 years old that have had a coronary artery calcification score determined by rapid computed tomography at the clinical site within the last six months.
排除标准
- •Receiving investigational treatments
- •Psychosocial issues that interfere with an ability to follow study procedures
- •Known to be pregnant
- •Receiving dialysis or having known renal compromise
- •Scars, tattoos, rashes or other disruption/discoloration on the left volar forearm.
- •Recent or current oral steroid therapy or topical steroids applied to the left forearm
- •Current chemotherapy, or chemotherapy within the past 12 months
- •Receiving medications that fluoresce*
- •Known to have, or at risk for, photosensitivity reactions ( e.g., sensitive to ultraviolet light, or taking medication known to cause photosensitivity)
研究者
研究点 (1)
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