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CompletedNCT04711382

The Use of Faster Acting Aspart in Type 1 Diabetes Patients

The Use of Faster Acting Aspart in Type 1 Diabetes Patients: Multi-centre Real-world Experience

Status
Completed
Phase
Study type
Observational
Enrollment
438 (actual)
Sponsor
University Hospital, Antwerp · Academic / Other
Sex
All
Age
16 Years – 100 Years
Healthy volunteers
Not accepted

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.

Detailed 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

Conditions

Timeline

Start date
2018-01-29
Primary completion
2020-12-14
Completion
2021-01-01
First posted
2021-01-15
Last updated
2021-01-15

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT04711382. Inclusion in this directory is not an endorsement.

The Use of Faster Acting Aspart in Type 1 Diabetes Patients (NCT04711382) · Clinical Trials Directory