Type 2 Diabetes
Conditions
Keywords
Screening for Type 2 diabetes
Brief summary
The primary objective is to identify compare SCOUT DS to random capillary glucose for identification of at-risk subjects with dysglycemia defined by hemoglobin A1C ≥ 6.0%.
Detailed description
The study will complete up to 400 subjects at the clinical site to evaluate the precision and accuracy of SCOUT DS and random capillary glucose for detecting pre-diabetes and undiagnosed type 2 diabetes in subjects at risk but not having a pre-existing diagnosis of type 2 diabetes. A point of care A1c measurement will serve as the reference method for defining pre-diabetes (6.0% ≤ A1c ≤ 6.4%) and diabetes (A1c ≥ 6.5%). The study will require one visit by each subject to the clinical site. The visit does not require fasting and can be done any time of day. The study (not including the IRB process and recruiting) is expected to last 6 months. The target cohort for comprises persons at risk for pre-diabetes and/or type 2 diabetes.
Interventions
None listed
Sponsors
VeraLight, Inc.
Greece National Social Insurance Institute
Laikο General Hospital, Athens
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Age greater than or equal to 45 years OR Age 18 to 44 years and with one or more of the following risk factors: * BMI \> 25 kg/m² * 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 * Ethnicity with elevated risk for type 2 diabetes * 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
Exclusion criteria
* • Under 18 years of age * 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 with the exception of metformin * 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)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Comparison of SCOUT DS to Random Capillary Glucose | Up to 6 months | A point of care A1c measurement will serve as the reference method for defining pre-diabetes (6.0% ≤ A1c ≤ 6.4%) and diabetes (A1c ≥ 6.5%). The study will require one visit by each subject to the clinical site. The visit does not require fasting and can be done any time of day. The study (not including the IRB process and recruiting) is expected to last 6 months. The target cohort for comprises persons at risk for pre-diabetes and/or type 2 diabetes. |
Countries
Greece
Outcome results
None listed