Develop Novel Methods to Display, Report and Analyze CGM Data for Clinical Decision-Making in People With Diabetes

Completed

Conditions studied: Diabetes, Glucose Variability, CGM

In brief

The purpose of this study is to obtain sufficient continuous glucose monitoring (CGM) data in a manner that provides clinical information that is not available using conventional self-monitored blood glucose. Currently, a formal method does not exist for evaluating CGM data except for looking at each glucose reading across the days a CGM system has been worn and evaluating it based on clinical practice experience. The hope is that a mathematical model can be developed that will enable health care providers to quickly and easily determine what changes in diabetes treatment need to be made after CGM data is obtained.

Key facts

Study ID

NCT00465881

Run by

HealthPartners Institute

People needed

30

Starts

2006-01-01

Expected to finish

2006-04-01

Last updated by the study team

2015-12-03

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female
• Diagnosed with type 1 or type 2 diabetes
• Treated with insulin therapy
• Can also be taking other diabetes medication treatment
• Age 21 and older
• Willing to give informed consent
• Capable of following the protocol and instructions of study staff
• Available for scheduled visits
• Access to telephone communications

You may not qualify if…

• Under 21 years of age
• Unable to follow protocol
• Unable to read and write in English
• Skin abnormalities at insertion sites
• Allergy to adhesives
• Any concomitant medication thay would likely affect evaluation of device

Where it is running

• International Diabetes Center - Park Nicollet Health Services — Minneapolis, Minnesota, United States

Full record on ClinicalTrials.gov

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