System Accuracy and User Performance of Blood Glucose Monitoring Systems for Self-Testing in Managing Diabetes Mellitus

B. Braun

Status: Completed

Conditions: Diabetes

Treatments: Device: Blood glucose monitoring system (Omnitest 5); Device: Blood glucose monitoring system (Omnitest 3); Device: Blood glucose monitoring system (Omnitest 5D)

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT02290067

IDT-1340-BE (Other Identifier)

OPM-G-V-1203

Details and patient eligibility

About

The aim of this test is to determine the system accuracy and user performance evaluation of three Blood Glucose Monitoring systems. For system accuracy evaluation the measurement data should cover the whole range of glucose concentration which could usually be expected in patients with diabetes mellitus.

Enrollment: 130 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Subjects with type 1 or type 2 diabetes and healthy subjects
• Signed and dated informed consent form
• For small modifications of the insulin doses to achieve certain blood glucose values (system accuracy evaluation): Male or female subjects with diabetes mellitus type 1 with intensified insulin therapy (intensified conventional therapy) or insulin pump therapy (continuous subcutaneous insulin infusion)

Exclusion criteria

• Pregnancy or lactation period
• Severe acute illness that in the opinion of the investigating physician might confound the results of the test or which could result in a risk to the patient caused by the test
• Mental incapacity or language barriers precluding adequate compliance with the test procedures
• Severe chronic illness besides diabetes mellitus as assessed by the investigating physician that might confound the results of the test or which could result in a risk to the patient caused by the test
• Legal incompetence or limited legal competence
• Dependency from the sponsor or the clinical investigator (e.g. coworkers of the sponsor or the clinical research center)
• For user performance evaluation: Subjects having used the test systems before themselves or having participated in a study with these Blood Glucose Monitoring Systems
• For system accuracy evaluation: subjects intended to provide blood samples with glucose concentrations between 50 and 80 mg/dl must not have coronary heart disease, myocardial infarction in history, cerebral events in history, peripheral artery occlusive disease- or impaired hypoglycaemia awareness

Trial design

Primary purpose: Diagnostic

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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130 participants in 3 patient groups

Omnitest 3

Active Comparator group

Description:

Blood glucose monitoring system

Treatment:

Device: Blood glucose monitoring system (Omnitest 3)

Omnitest 5

Experimental group

Description:

Blood glucose monitoring system

Treatment:

Device: Blood glucose monitoring system (Omnitest 5)

Omnitest 5D

Experimental group

Description:

Blood glucose monitoring system

Treatment:

Device: Blood glucose monitoring system (Omnitest 5D)