Evaluation of an Ascensia Blood Glucose Meter and App System
| Status: | Completed |
|---|---|
| Conditions: | Diabetes, Diabetes |
| Therapuetic Areas: | Endocrinology |
| Healthy: | No |
| Age Range: | 18 - 75 |
| Updated: | 8/26/2017 |
| Start Date: | October 2015 |
| End Date: | November 2015 |
Open Label, Single-center Study of the Onyx Meter and App System for Blood Glucose Monitoring in Insulin-Dependent and Insulin-using, Non-Insulin-Dependent Diabetes Mellitus Patients to Demonstrate Usability in a Clinical Setting.
The purpose of this study is to assess the usability of the Onyx system in the hands of
subjects with Insulin Dependent Diabetes Mellitus (IDDM) or insulin-using subjects with
Non-IDDM.
subjects with Insulin Dependent Diabetes Mellitus (IDDM) or insulin-using subjects with
Non-IDDM.
Inclusion Criteria:
- Be aged 18-75 years, male or female
- Read and understand English
- Have diagnosis of type 1 or insulin-using type 2 diabetes for at least 6 months
- Be taking multiple daily injections (MDI) of at least two pre-meal bolus injections
daily or using an insulin pump
- Performing self-monitoring of blood glucose at home at least twice daily
- Have an iOS mobile device or Android mobile device with blue tooth capability
- iOS device: iPod or iPhone 5 or later version with iOS 8.0 software or higher (no
tablets)
- Android: smart phone, 4.4 version and higher (no tablets)
- Be willing to utilize the ONYX App on personal mobile device which communicates to
meter to manage diabetes (including use of the bolus calculator)
- Be ambulatory and have transportation to the study site
Exclusion Criteria:
- Hemophilia or any other bleeding disorder
- Pregnancy
- Physical, visual or neurological impairments that would make the person unable to
perform testing with the BGM
- 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.
- A condition, which in the opinion of the investigator or designee, would put the
person or study conduct at risk (reason for exclusion will be clearly documented by
investigator or designee on the subject disposition form).
- Proliferative retinopathy or history of retinal laser surgery
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