Evaluation of the MiniMed™ 780G System in Type 1 Adult and Pediatric Subjects Utilizing Insulin Fiasp®

NCT05224258 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 240

Last updated 2025-06-22

Study results available
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Summary

This global study (US, Canada, and Australia) will evaluate the safety and effectiveness of the MiniMed 780G system in type 1 adult and pediatric subjects utilizing Fiasp (insulin aspart injection) in a home setting.

Conditions

Interventions

DEVICE

MiniMed 780G System

780G System used with Insulin Fiasp® (Insulin Aspart Injection)

Sponsors & Collaborators

  • Medtronic Diabetes

    lead INDUSTRY

Principal Investigators

  • David Liljenquist, MD · Rocky Mountain Clinical Research

  • Mark Warren, MD · Physicians East

  • John Reed, MD · Endocrine Research Solutions

  • Frances Broyles, MD · Rainier Clinical Research Center

  • Dorothy Shulman, MD · University of South Florida

  • Bruce Bode, MD · Atlanta Diabetes Associates

  • Halis Akturk, MD · University of Colorado, Denver

  • Paul Norwood, MD · Valley Research

  • Carla Demeterco-Berggren, MD · Rady's Children's Hospital

  • Alexander Abitbol, MD · LMC Clinical Research

  • Daniele Pacaud, MD · Alberta Children's Hospital Research Institute

  • James Thrasher, MD · Medical Investigations, Inc.

  • Bhuvana Sunil, MD · MultiCare Institute for Research & Innovation

  • Mark Kipnes, MD · Diabetes and Glandular Disease Clinic, P.A.

  • Asheesh Dewan, MD · The Docs LLC

  • Barry Reiner, MD · Barry J Reiner MD LLC

  • Gnanagurudasan Prakasam, MD · Sutter Institute for Medical Research

  • Bruce King, MD · John Hunter Childrens Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
7 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-03-17
Primary Completion
2024-06-21
Completion
2024-06-21
FDA Device
Yes

Countries

  • United States
  • Australia
  • Canada

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05224258 on ClinicalTrials.gov