CGM Use in Poorly Controlled Youth With Type 1 Diabetes (IMPaCT)

Johns Hopkins University

Status: Completed

Conditions: Hypoglycemia; Type 1 Diabetes; High Blood Sugar

Treatments: Device: Dexcom G6 Continuous Glucose Monitor

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT04721145

IRB00255470

Details and patient eligibility

About

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.

Enrollment: 26 patients

Sex: All

Ages: 5 to 21 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Diagnosis of Type 1 diabetes for >3 months

Exclusion criteria

• CGM use in the last 6 months

Trial design

Primary purpose: Supportive Care

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

---

26 participants in 1 patient group

Dexcom G6 Continuous Glucose Monitor

Experimental group

Description:

Children with type 1 diabetes will wear a continuous glucose monitor (CGM) for 10 days.

Treatment:

Device: Dexcom G6 Continuous Glucose Monitor