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
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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