The Use of Faster Acting Aspart in Type 1 Diabetes Patients

Status Completed

Clinical Trial Summary

Data on switching from traditional mealtime insulins to fast-acting insulin aspart (Fiasp) in routine clinical practice are sparse. The aim was to evaluate the efficacy and safety of switching from traditional mealtime insulin to Fiasp in a "real-world" clinical practice setting in people with type 1 diabetes in Belgium.

Clinical Trial Description

The primary endpoint was the evolution of time in range (TIR, 70-180 mg/dl) at 6 and 12 months. Secondary endpoints included change in HbA1c, BMI, insulin doses, time below range (T<70 and T<54 mg/dl) and time above range (T>180 and T>250 mg/dl). Retrospective analysis Two-center study ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04711382
Study type	Observational
Source	University Hospital, Antwerp
Contact
Status	Completed
Phase
Start date	January 29, 2018
Completion date	January 1, 2021

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