Diabetes
Conditions
Brief summary
Performance Evaluation by the User of the Blood Glucose Monitoring SystemContour Care in accordance with DIN EN ISO 15197:2015
Interventions
DIAGNOSTIC_TESTblood glucose measurement by subject
blood glucose measurement by subject using finger tip capillary blood
Sponsors
Institut fur Diabetes Karlsburg GmbH
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Male or female patients with clinical indication for blood glucose measurements (i.e. Diabetes mellitus) * Male or female patients with hypo-, eu- or hyperglycemia * The written informed consent had to be signed * The volunteers must be older than 18 years * The volunteers have legal capacity and are able to understand meaning, nature and possible consequences of the procedures involved
Exclusion criteria
* Pregnancy or lactation * Acute or chronic diseases that * pose a risk of aggravation by the measure * pose a health hazard to the personnel * A current constitution that does not allow participating in the study * Participation in another study or activity with the blood glucose measuring system evaluated in the present study * Application of substances listed in Appendix A of DIN EN ISO 15197:2015
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Analysis of system accuracy based on DIN EN ISO 15197 | Day 1 | Assessment of the analytical measurement performance of the blood glucose monitor |
Countries
Germany
Outcome results
None listed