A Clinical Study of the C8 MediSensors Optical Glucose Monitor™

Completed · Not applicable

Conditions studied: Diabetes Mellitus

In brief

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.

Key facts

Study ID

NCT01726114

Run by

C8 MediSensors, Inc.

People needed

86

Starts

2012-06-01

Expected to finish

2013-03-01

Last updated by the study team

2013-03-26

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18 years of age or older.
• Understands and agrees to comply with study instructions.
• Read, understood, signed and dated the Informed Consent Form.

You may not qualify if…

• Pregnancy.
• Extensive skin changes or diseases that preclude wearing the test device at the proposed wear site(s) (e.g., extensive psoriasis, recent burns or severe sunburn, extensive eczema, extensive scarring, extensive tattoos, dermatitis herpetiformis).
• Employed by a company within the diabetes field other than the study sponsor.
• Medical history or any condition that may, in the opinion of the investigator, compromise the subject's ability to participate.

Where it is running

• C8 MediSensors, Inc. — San Jose, California, United States

Full record on ClinicalTrials.gov

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