Evaluation of Fiasp (Fast Acting Insulin Aspart) in 670G Hybrid Closed-Loop Therapy

  • STATUS
    Not Recruiting
  • participants needed
    20
  • sponsor
    Stanford University
Updated on 23 January 2021
diabetes
insulin
hemoglobin a1c
glycosylated hemoglobin
novolog
fiasp

Summary

This is a pilot outpatient study conducted at Stanford to obtain preliminary data on how Fiasp works in a closed-loop system and to determine if any changes need to be made to the 670G pump to optimize the use of Fiasp.

Description

This will be a randomized cross-over blinded study and to see how the 670G pump responds to the introduction of Fiasp insulin. Subjects enrolled in the study will have a 2 week period of optimization with weekly assessments of their Carelink download before entering the blinded phase of the study. They will use their usual home insulin during the optimization phase. They will then be started on their first blinded insulin (aspart or Fiasp) which they will use for 2 weeks, before they cross-over to the other insulin.

Details
Condition Insulin dependent diabetes mellitus
Treatment Fiasp, Novolog
Clinical Study IdentifierNCT03554486
SponsorStanford University
Last Modified on23 January 2021

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