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Metabolic Syndrome Feasibility Study (EPIC-009)

E

Epic Research & Diagnostics

Status

Completed

Conditions

Metabolic Syndrome

Study type

Observational

Funder types

Industry

Identifiers

NCT02287766
EPIC-009

Details and patient eligibility

About

The objective of this study is to determine whether the finger tip images captured by the EPIC ClearView device, when analyzed via the ClearView software, produce a Response Scale that characterizes trends consistent with Metabolic Syndrome identified by medical doctors.

Enrollment

193 patients

Sex

All

Ages

21 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Metabolic Group

Inclusion Criteria:

  1. Sex: Male or Female

  2. Age range: 21 to 85

  3. Qualifying Metabolic Syndrome diagnosis(using the National Cholesterol Education Program Adult Treatment Panel (ATP) III definition)(Grundy, 2004)

    Subjects will be identified as having Metabolic Syndrome if they meet at least three of the following five criteria:

    • Elevated waist circumference: ≥ 102 cm (≥40 inches) in men, ≥ 88 cm (≥35 inches) in women
    • Elevated triglycerides: ≥ 150 mg/dL (1.7 mmol/L) or on drug treatment for elevated triglycerides (examples include, but are not limited to, fibrates and nicotinic acid)
    • Reduced HDL cholesterol: < 40 mg/dL (1.03 mmol/L) in men or < 50 mg/dL (1.3 mmol/L) in women or on drug treatment for reduced HDL-C
    • Elevated blood pressure: ≥ 130 mm Hg systolic blood pressure or ≥85 mm Hg diastolic blood pressure or on antihypertensive drug treatment in a patient with a history of hypertension
    • Elevated fasting glucose: ≥ 100 mg/dL or on drug treatment for elevated glucose
  4. The patient or legal representative is able to understand and provide signed consent for the procedure.

Exclusion Criteria:

  1. Patients < 21years in age or > 85 years in age.
  2. Inability or unwillingness to provide informed consent.
  3. Patients with pacemakers or another electrical device implanted somewhere in their body.
  4. Pregnant women.
  5. Missing all or part of fingers or cuts/burns on pads of fingers
  6. Hand tremors or involuntary oscillations of the hands that prevents clear imaging

Control Group:

Inclusion Criteria:

  1. Sex: Male or Female
  2. Age range: 21 to 85
  3. Freedom from qualifying medical diagnoses (control group)

Any one of the following will exclude the subject from participation in the study

  1. Documented current diagnosis/treatment of cancer (including Sickle Cell Disease)
  2. Documented current diagnosis/treatment of coronary artery disease or heart attack
  3. Documented as currently in Renal Failure (chronic or acute) or on renal dialysis
  4. Documented current diagnosis/treatment for Hepatitis

5 .The patient or legal representative is able to understand and provide signed consent for the procedure.

Exclusion Criteria:

  1. Patients < 21 years in age or > 85 years in age.
  2. bility or unwillingness to provide informed consent.
  3. Patients with pacemakers or another electrical device implanted somewhere in their body.
  4. Pregnant women.
  5. Missing all or part of fingers or cuts/burns on pads of fingers
  6. Hand tremors or involuntary oscillations of the hands that prevents clear imaging

Trial design

193 participants in 2 patient groups

Control
Description:
Men and women ages 21-85 lacking any medical diagnosis (as defined in the protocol) of one or more of the following cancer, coronary artery disease or heart attack, renal failure or dialysis, hepatitis, Multiple Sclerosis, or any autoimmune disorder.
Metabolic Syndrome Diagnosis Group
Description:
Men and women ages 21-85 with at least of at least three of the following (as defined in the protocol) : Elevated waist circumference, elevated triglycerides, reduced HDL cholesterol, elevated blood pressure, elevated fasting glucose.

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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