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A Clinical Study of the C8 MediSensors Optical Glucose Monitor™

NCT01726114 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 86

Last updated 2013-03-26

No results posted yet for this study

Summary

The purpose of this study is to compare glucose measurements from the C8 MediSensors non-invasive Optical Glucose Monitor™ System to blood glucose measurements from the Yellow Springs Instrument(YSI) blood glucose analyzer.

Conditions

Interventions

DEVICE

Non-invasive Optical Glucose Monitor™

Test device

DEVICE

YSI blood glucose analyzer

Reference device

Sponsors & Collaborators

  • C8 MediSensors, Inc.

    lead INDUSTRY

Principal Investigators

  • Vice President, Clincal, Regulatory, Quality · C8 MediSensors, Inc.

Study Design

Allocation
NA
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2013-03-31
Completion
2013-03-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01726114 on ClinicalTrials.gov