Trials / Completed
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.