Continuous Glucose Monitoring Self-Monitored Blood Glucose Type 2 Therapy Matrix Definition
Completed
Conditions studied: Diabetes Mellitus, Type 2, Diabetic Blood Glucose Monitoring
In brief
The purpose of this study is to use data from the Continuous Glucose Monitoring (CGM) device and your Self-Monitored Blood Glucose (SMBG) levels to determine the best times to test blood glucose levels using SMBG.
Key facts
- Study ID
- NCT01390610
- Run by
- HealthPartners Institute
- People needed
- 27
- Starts
- 2011-06-01
- Expected to finish
- 2013-01-01
- Last updated by the study team
- 2015-11-26
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or female
- Diagnosed with type 2 diabetes and treated with diabetes medication(s) as required by the protocol (See Section 3.1)
- Age 18 and older
- Willing to give informed consent
- Motivated and capable of following the protocol and instructions provided by the healthcare professional
- Available for the study on the scheduled visit days
- Have not participated in a prior research trial at IDC that utilized CGM
You may not qualify if…
- Under 18 years of age
- Skin abnormalities at the CGM insertion sites that would confound assessment of the effect of the device on the skin
- Allergy to adhesives
- Taken prednisone or cortisone medications in the previous 30 days
- Currently pregnant or planning pregnancy during the study period
- Presence of any severe medical or psychological condition or chronic conditions/infections that in the opinion of the Investigator would compromise the subject's safety or successful participation in the study
- Unable to follow the study protocol
- Unable to speak, read and write in English
Where it is running
- International Diabetes Center — Minneapolis, Minnesota, United States
Full record on ClinicalTrials.gov
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