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Continuous Glucose Monitor in Children With Poorly Controlled Diabetes

NCT02530450 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2017-10-06

Study results available
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Summary

The purpose of this study is to determine if the use of continuous glucose monitoring in a practical outpatient clinic setting in children with poorly controlled diabetes will lead to improved blood sugar control.

Conditions

  • Type 1 Diabetes Mellitus

Interventions

DEVICE

continuous glucose monitoring (CGM)

All subjects in Groups 1 and 2 wore the CGM device at time points 0, 3 months, and 6 months. Group 1 did not review CGM data at time 0, but did review CGM data at time point 3 months and 6 months. Group 2 reviewed CGM data at all time points.

Sponsors & Collaborators

  • Medtronic Diabetes

    collaborator INDUSTRY

  • The University of Texas Health Science Center at San Antonio

    lead OTHER

Principal Investigators

  • Maria Rayas, MD · UT Health Science Center San Antonio

Eligibility

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

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2013-03-31
Completion
2013-03-31

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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 NCT02530450 on ClinicalTrials.gov