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Paediatric Use of the Abbott Sensor Based Glucose Monitoring System

NCT03433573 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 103

Last updated 2018-08-29

No results posted yet for this study

Summary

Accuracy evaluation of the Abbott Sensor Based Glucose Monitoring System when used by children with diabetes.

Conditions

Interventions

DEVICE

Abbott Sensor Based Glucose Monitoring System

Subjects will wear the Abbott Sensor Based Glucose Monitoring System and will be asked to perform 4 blood glucose tests per day (pre-meal and before bedtime). Subjects will be asked to scan the sensor when each blood glucose test is performed.

Sponsors & Collaborators

  • Abbott Diabetes Care

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
4 Years
Max Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-16
Primary Completion
2018-05-11
Completion
2018-05-11

Countries

  • United Kingdom

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 NCT03433573 on ClinicalTrials.gov