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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04721145
Other study ID # IRB00255470
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 25, 2021
Est. completion date June 28, 2022

Study information

Verified date July 2023
Source Johns Hopkins University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this prospective study is to determine if trial use of a Dexcom G6 CGM system for a 10 day wear period in high risk, poorly controlled pediatric Type 1 diabetes patients increases uptake of personal CGM use, and improves short-term time in range glucose control.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date June 28, 2022
Est. primary completion date June 28, 2022
Accepts healthy volunteers No
Gender All
Age group 5 Years to 21 Years
Eligibility Inclusion Criteria: - Diagnosis of Type 1 diabetes for >3 months Exclusion Criteria: - CGM use in the last 6 months

Study Design


Intervention

Device:
Dexcom G6 Continuous Glucose Monitor
Eligible patients will have a Dexcom G6 Continuous Glucose Monitor placed for 10 days.

Locations

Country Name City State
United States Johns Hopkins Pediatric Diabetes Center Baltimore Maryland

Sponsors (2)

Lead Sponsor Collaborator
Johns Hopkins University DexCom, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Personal CGM Use Evaluate whether there is any change in uptake of personal CGM after 10-day trial. Baseline and 3 months
Secondary Change in the Percent Time in Range Glucose Control Changes in time in range glucose control from 1-5 days to 6-10 days from the Dexcom CGM 1-5 days and 6-10 days
Secondary Change in Hemoglobin A1c Changes in HbA1c from baseline to next available A1c at 3-6 month follow up visit Baseline, 3-6 months
Secondary Using Personal CGM Percentage of participants using CGM at time of follow up, of those who reported wanting a personal CGM 3-6 months
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