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临床试验/NCT01080157
NCT01080157已完成不适用

An Evaluation of a Noninvasive Diabetes Screening Device in Subjects at Risk for Diabetes

VeraLight, Inc.12 个研究点 分布在 1 个国家目标入组 509 人开始时间: 2010年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
509
试验地点
12
主要终点
Validation of SCOUT DS algorithm, ROC performance equivalency to FPG and A1c for detection of abnormal glucose tolerance.

研究概览

简要总结

The purpose of this research study is to test the safety and effectiveness of the SCOUT DS in measuring the concentration of substances (advanced glycation endproducts) in the skin. These substances have been found to be in higher concentrations in people with diabetes and high blood sugar. The SCOUT DS is being developed to help doctors measure these substances in skin and possibly help doctors diagnose diabetes.

详细描述

The trial will be a prospective, multi-center, paired data, cohort screening trial. Up to 960 subjects will complete the study to determine the relative accuracy of SCOUT DS compared to the FPG and HbA1c tests in screening for abnormal glucose tolerance. All methods will be compared to the 2 hour value of the OGTT. An algorithm utilizes skin optical modeling as well as the spectral and blood assay data accumulated from the initial phase of the study to produce a risk score for abnormal glucose tolerance. This algorithm and the calculation of the score will be integrated into the SCOUT DS for prospective testing. The design requires three patient visits to the clinical site and up to a total of seven measurements on the SCOUT device.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age greater than or equal to 45 years; OR
  • Age 18 to 44 years and a BMI > 25 kg/m² with one or more of the following risk factors:
  • Elevated waist circumference, > 35 inches for women and >40 inches for men
  • Habitually physically inactive (does not exercise regularly)
  • Has a first-degree relative with diabetes
  • African American, Latino, Native American, Asian American, Pacific Islander
  • Has delivered a baby weighing > 9 lb or diagnosed with gestational diabetes
  • Hypertension (≥130/≥ 85 mmHg) or being treated for hypertension
  • HDL cholesterol level < 35 mg/dL and/or a fasting triglyceride level ≥ 250 mg/dL or being treated for dyslipidemia with medication
  • Has been previously diagnosed with Polycystic Ovary Syndrome (PCOS)
  • Had impaired glucose tolerance or impaired fasting glucose on previous testing within the last 3 yrs
  • Conditions associated with insulin resistance such as acanthosis nigricans
  • History of vascular disease including heart attack, stroke, angina, coronary heart disease, atherosclerosis, congestive heart failure or peripheral arterial disease

排除标准

  • Prior participation in VL-2701
  • Receiving investigational treatments in the past 14 days
  • Psychosocial issues that interfere with an ability to follow study procedures
  • Conditions that cause secondary diabetes including Cushing's syndrome, acromegaly, hemochromatosis, pancreatitis, or cystic fibrosis
  • Diagnosed with any type of diabetes, including type 1 or 2
  • Taking glucose lowering medications
  • Known to be pregnant
  • Receiving dialysis or having known renal compromise
  • Scars, tattoos, rashes or other disruption/discoloration on the left volar forearm.
  • Recent (within past month) or current oral steroid therapy or topical steroids applied to the left forearm; inhaled steroid therapy is not excluded 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)
  • Prior bariatric surgery

结局指标

主要结局

Validation of SCOUT DS algorithm, ROC performance equivalency to FPG and A1c for detection of abnormal glucose tolerance.

时间窗: Outcome measure is determined 2-3 months after completion of Visit 3

The relative true positive and relative true negative fractions between the SCOUT DS and FPG tests for detecting abnormal glucose tolerance (2 hr OGTT value ≥ 140 mg/dL)

次要结局

  • Receiver operator characteristic area under the curve, sensitivity, specificity, and postive & negative predictive values of the SCOUT DS, FPG, and A1C tests for detection of abnormal glucose tolerance, and the intra- & inter-day SCOUT DS test(Outcome measure is determined 2-3 months after completion of Visit 3)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (12)

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