AIDANET Pediatrics Study for Type 1 Diabetes

This study is testing the AIDANET system, an automated insulin delivery system, in children aged 6 to 13 years old with Type 1 Diabetes. The AIDANET system uses a smartphone-based control, a modified Tandem insulin pump, and a Dexcom G6 continuous glucose monitor (CGM). Researchers want to see if two different settings of the AIDANET system – a Normal Glycemia Goal and a Tight Glycemia Goal – are as good as usual care in managing blood sugar levels. You could be eligible if you are between 6 and 13 years old, have had Type 1 Diabetes for at least one year, and have been using an insulin pump for at least three months and insulin for at least six months. The study plans to enroll 42 participants, and its current status is unclear.

Study design
This is an interventional study, meaning participants will receive a specific intervention. It plans to enroll 42 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
The primary endpoint is measured at 28 days, which suggests a follow-up period of at least this length.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07020936

AIDANET Pediatrics

Active, Not Recruiting
NAAges 6–13InterventionalTreatment
Mark D. DeBoer, MD, MSc., MCR
~42 participants
Updated 2026-06-01 on ClinicalTrials.gov
What's tested:Normal Glycemia GoalTight Glycemia Goal

At a glance

Recruiting sites
0 of 3 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Non-inferiority of mean CGM between FCL and Usual Care
Measured over 28 days
Type 1 Diabetes
3 sites across 3 states
California1
Colorado1
Virginia1
  • Mark DeBoer, MD · STUDY_CHAIR · University of Virginia Center for Diabetes Technology

This trial hasn't published a contact. View it on ClinicalTrials.gov

  • Non-inferiority of mean CGM between FCL and Usual Care28 days

    Non-inferiority of the mean CGM between the two weeks of the Usual Care observational period and the two weeks of AIDANET at-home