Comparison Evaluation of Blood Glucose Meter Systems in a Clinical Setting

Completed · Not applicable

Conditions studied: Diabetes

In brief

The purpose of this study was to test the performance of an investigational Bayer Blood Glucose (BG) meter and five additional Blood Glucose Monitoring Systems (BGMSs). The goal was to obtain glucose samples from subjects with diabetes across the meter operating ranges. A capillary sample was collected from each subject at 3 different times during the visit to obtain natural capillary blood samples with a range of glucose concentrations. Some blood samples were glycolyzed to lower the glucose concentration levels and glucose solution was added to other samples to raise glucose concentration levels. All meter BG results were compared with plasma results obtained with a reference laboratory glucose method (YSI Glucose Analyzer). All lancings and testing were performed by study staff.

Key facts

Study ID

NCT01614613

Run by

Ascensia Diabetes Care

People needed

146

Starts

2012-05-01

Expected to finish

2012-06-01

Last updated by the study team

2016-02-29

Who can join

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

You may qualify if…

• Diagnosis of type 1 or type 2 diabetes mellitus
• 18 years of age or older
• Willing to follow all study procedures

You may not qualify if…

• Received an investigational drug or device within the last 30 days
• Current use or recent exposure to any prescription medication within 24 hours prior to screening that in the opinion of the investigator could have an influence on the subject's ability to participate in the study or on the performance on the test device
• Positive pregnancy test obtained at screening (test performed for females only, except if surgically sterile or three years past menopause)
• Hematocrit <32% or >55%
• Inadequate veins (in the opinion of the investigator or designated study staff) for venous blood withdrawal or intravenous catheter insertion
• Symptomatic coronary artery disease with a history of angina, or history of a myocardial infarction or coronary intervention (e.g. percutaneous transluminal coronary angioplasty [PTCA], stent placement) or coronary artery bypass graft (CABG) within the past 6 months
• Cerebrovascular accident within the past 6 months
• Diagnosis of the following diabetic autonomic neuropathies: symptomatic orthostatic hypotension, heart rate anomalies, gastroparesis
• Being treated for malignancy, except basal cell or squamous cell skin cancers
• Major surgical operation within 30 days prior to screening
• Active alcohol abuse or substance abuse (as judged by the principal investigator)
• Severe mental illness, mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation (as judged by principal investigator)
• Other medical conditions that would pose safety concerns, interfere with study conduct or seriously compromise study integrity, as judged by principal investigator (reason for exclusion will be clearly documented by investigator or designee)
• Working for a competitive medical device company, or having an immediate family member or someone who is not a family member but is living within the household of someone who works for such a company

Where it is running

• Rainier Clinical Research Center Inc — Renton, Washington, United States

Full record on ClinicalTrials.gov

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