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System Accuracy of the Blood Glucose Monitor for Personal Use Contour Care

NCT06037551 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 105

Last updated 2025-04-17

No results posted yet for this study

Summary

This study assesses the system accuracy of a blood glucose monitoring system in accordance with DIN EN ISO 15197:2015

Conditions

Interventions

DIAGNOSTIC_TEST

blood glucose measuremen subject

measurement of the blood glucose concentration of subject using BGM and capillary finger tip blood

DIAGNOSTIC_TEST

blood glucose measuremen reference

measurement of the blood glucose concentration of subject using reference method and capillary finger tip blood

Sponsors & Collaborators

  • Institut fur Diabetes Karlsburg GmbH

    lead OTHER

Principal Investigators

  • Kerstin Rebrin, PhD · Institut fur Diabetes Karlsburg GmbH

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-01
Primary Completion
2023-11-01
Completion
2023-11-30

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06037551 on ClinicalTrials.gov