NCT01346046已完成不适用
An Evaluation of a Noninvasive Diabetes Screening Device in Subjects at the TCOYD Diabetes Conference
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 264
- 试验地点
- 1
- 主要终点
- Continuing validation of SCOUT DS algorithm
研究概览
简要总结
The primary objective of the trial is to collect SCOUT DS and Hemoglobin A1c measurements of subjects who have been diagnosed with Type 2 diabetes.
详细描述
Previous studies have excluded subjects with Type 2 diabetes. The primary objective of this study is to correct an imbalance in the disease prevalence of the data set used to develop the SCOUT DS diabetes screening algorithm.
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
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Age greater than or equal to 18 years Self-reported diagnosis of type 2 diabetes No Self-reported diagnosis of type 2 diabetes
排除标准
- •Less than 18 years of age
- •Diagnosed with type 1 diabetes
- •Known to be pregnant (Self Reported)
- •Receiving dialysis or having known renal compromise
- •Scars, tattoos, rashes or other disruption/discoloration on the left volar forearm.
- •Known to have, or at risk for, photosensitivity reactions ( e.g., sensitive to ultraviolet light, or taking medication known to cause photosensitivity)
结局指标
主要结局
Continuing validation of SCOUT DS algorithm
时间窗: 1 day
Collect SCOUT DS and Hemoglobin A1c measurements of subjects with Type 2 Diabetes
次要结局
未报告次要终点
研究者
研究点 (1)
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