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Completed No phase listed Observational Accepts healthy volunteers

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

ClinicalTrials.gov ID: NCT01080157

Public ClinicalTrials.gov record NCT01080157. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 7, 2026, 11:53 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT01080157
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
VeraLight, Inc.
Industry
Enrollment
509 participants

Conditions and interventions

Conditions

Interventions

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 2010 (Type not available)
Primary completion
Dec 2010 (Actual)
Completion
Dec 2010 (Actual)
Last update posted
Dec 4, 2012

2010

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
11
Facility City State ZIP Site status
Accelovance - Huntsville Huntsville Alabama 35802 —
Accelovance - San Diego, CA San Diego California 92108 —
Radiant Research, Inc. - Chicago Chicago Illinois 60654 —
Accelovance - Peoria, IL Peoria Illinois 61602 —
Radiant Research, Inc. - Kansas City Kansas City Kansas 66202 —
Accelovance - Rockville, MD Rockville Maryland — —
Radiant Research, Inc. - Minneapolis Minneapolis Minnesota 55345 —
Lovelace Scientific Resources, Inc. Albuquerque New Mexico 87108 —
Radiant Research, Inc. - Cincinnati Cincinnati Ohio 45249 —
Juno Research, LLC Houston Texas 77036 —
Dynamed Clinical Research, LP Houston Texas 77375 —
Radiant Research, Inc. - San Antonio San Antonio Texas 78229 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01080157, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 4, 2012 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01080157 live on ClinicalTrials.gov.

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