The Use of Faster Acting Aspart in Type 1 Diabetes Patients
- Conditions
- Type 1 DiabetesInsulinTime in Range
- Registration Number
- NCT04711382
- Lead Sponsor
- University Hospital, Antwerp
- Brief 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
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 438
- Type 1 diabetes patients
- Duration of diabetes > 2 years
- Using CGM for > 6 months
- Using SMBG
- Pregnancy
- Using glucocorticoids or immunosuppressive agents
- Active oncological problem
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time in Range 12 months Time in target range at 12 months
- Secondary Outcome Measures
Name Time Method Time in Range 6 months Time in target range at 6 months
Change in HbA1c 6 months & 12 months Change in HbA1c
Coefficient of variation 6 months & 12 months Change in coefficient of variation
Change in weight 6 months & 12 months Change in weight
Time above range 6 months & 12 months Change in time above range
Time below range 6 months & 12 months Change in time below range
Change in insulin doses 6 months & 12 months Change in insulin doses
Trial Locations
- Locations (1)
Antwerp University Hospital
🇧🇪Edegem, Antwerp, Belgium