At a glance
ClinicalIndex Comparison RecordN/ACompleted· 26 enrolled
Drug / intervention
Dexcom G6 Continuous Glucose Monitordevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
IMPaCT: IMPlementing Continuous Glucose Monitoring in High-risk, Poorly Controlled Children With Type 1 Diabetes
In Brief
A clinical study evaluating Dexcom G6 Continuous Glucose Monitor for Type 1 Diabetes and 2 related conditions. Completed, enrolled 26 participants across 1 site.
Detailed 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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsType 1 Diabetes, Hypoglycemia, High Blood Sugar
CountriesUnited States
CollaboratorsDexCom, Inc.
Timeline
N/ACompletedFinished
202120222023202420252026
First PostedJan 2021
Enrollment StartJan 2021
Primary CompletionJun 2022
TodayJul 2026
First PostedJan 22, 2021
Enrollment StartJan 25, 2021
Primary CompletionJun 28, 2022
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 5.4 years ago
Interventions
Dexcom G6 Continuous Glucose Monitordevice
Eligible patients will have a Dexcom G6 Continuous Glucose Monitor placed for 10 days.