POGO® Automatic Blood Glucose Monitoring System Clinical Study

Completed

Conditions studied: Diabetes Mellitus

In brief

The purpose of this study is to determine if the POGO® system delivers accurate blood glucose readings in the hands of the lay user and assess the POGO® system accuracy when used by trained health care professionals.

Key facts

Study ID

NCT02333864

Run by

Intuity Medical, Inc

People needed

287

Starts

2014-12-01

Expected to finish

2015-03-01

Last updated by the study team

2015-05-28

Who can join

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

You may qualify if…

• Be diagnosed with diabetes
• Be 18 years of age or older
• Be able to read, write, and understand English fluently
• Be able and willing to give written informed consent and have provided signed, written consent

You may not qualify if…

• Any condition which in the opinion of the Investigator may place the subject or site personnel at excessive risk
• A physical condition or limitation that prevents the subject from reading the labeling and using a BGMS on their own
• Previous experience with the POGO® BGMS
• Formal experience with clinical (medical) laboratory equipment or formal training in a relevant medical field

Where it is running

• Diablo Clinical Reasearch — Walnut Creek, California, United States
• Park Nicollett Institute - International Diabetes Center — Minneapolis, Minnesota, United States

Full record on ClinicalTrials.gov

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