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Continuous Glucose Monitor
Dexcom G6 Continuous Glucose Monitor for Type 1 Diabetes (IMPaCT Trial)
N/A
Waitlist Available
Led By Risa Wolf, MD
Research Sponsored by Johns Hopkins University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Diagnosis of Type 1 diabetes for >3 months
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3-6 months
Awards & highlights
IMPaCT Trial Summary
This study is evaluating whether a continuous glucose monitor may help improve glucose control in children with type 1 diabetes.
Eligible Conditions
- Type 1 Diabetes
- Low Blood Sugar
- High Blood Sugar
IMPaCT Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowIMPaCT Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3-6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3-6 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Personal CGM Use
Secondary outcome measures
Change in Hemoglobin A1c
Change in the Percent Time in Range Glucose Control
Using Personal CGM
IMPaCT Trial Design
1Treatment groups
Experimental Treatment
Group I: Dexcom G6 Continuous Glucose MonitorExperimental Treatment1 Intervention
Children with type 1 diabetes will wear a continuous glucose monitor (CGM) for 10 days.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Dexcom G6 Continuous Glucose Monitor
2021
N/A
~30
Find a Location
Who is running the clinical trial?
DexCom, Inc.Industry Sponsor
137 Previous Clinical Trials
29,826 Total Patients Enrolled
Johns Hopkins UniversityLead Sponsor
2,262 Previous Clinical Trials
14,823,138 Total Patients Enrolled
Risa Wolf, MDPrincipal InvestigatorJohns Hopkins University
1 Previous Clinical Trials
164 Total Patients Enrolled
Frequently Asked Questions
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