Performance Evaluation by the User of BGM Contour Care According to ISO 15197:2015

Institut fur Diabetes Karlsburg GmbH

Status: Completed

Conditions: Diabetes

Treatments: Diagnostic Test: blood glucose measurement by subject

Study type: Interventional

Funder types: Other

Identifiers

NCT06937736

2024_002

Details and patient eligibility

About

Performance Evaluation by the User of the Blood Glucose Monitoring SystemContour Care in accordance with DIN EN ISO 15197:2015

Enrollment: 101 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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101 participants in 1 patient group

Subject glucometer measurement

Experimental group

Description:

Blood glucose measurement BGM for personal use

Treatment:

Diagnostic Test: blood glucose measurement by subject