About this trial

The goal of this clinical trial is to evaluate the efficacy and safety of Medtronic 780G automated insulin delivery system in adult persons with type 1 diabetes and gastroparesis.

Eligibility criteria

Qualifiers

Age ≥18 years

Diagnosis of T1D for at least 12 months with stable insulin regimen for at least 2 months

HbA1c ≥8.0%

Diagnosis of gastroparesis per National Institute of Health (NIH) definition

Disqualifiers

Age <18 years

Current use of inhaled insulin (Afrezza)

Patients with T1D using any glucose lowering medications other than insulin at the time of screening

Pregnancy, breast feeding, or wanting to become pregnant

Trial design

Treatments tested in this trial

  • Medtronic 780G AID

Treatment groups

34 Participants
are divided into 2 treatment groups

Locations

1
Indiana University Health, Univeristy hospital46202, IndianapolisIndiana, United States

Sponsors and collaborators

Viral N. Shah

Lead sponsor

Indiana University

Sponsor institution

Medtronic

Collaborator