FiASP vs. aspart using an advanced closed-loop system
Not Applicable
Active, not recruiting
- Conditions
- type 1 diabetesMetabolic and Endocrine - Diabetes
- Registration Number
- ACTRN12619000469112
- Lead Sponsor
- Medtronic Diabetes
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Active, not recruiting
- Sex
- All
- Target Recruitment
- 24
Inclusion Criteria
Type 1 diabetes of >1 year duration
Stable on insulin pump therapy for >3 months
Proficient in carbohydrate counting
Continuous glucose monitoring (CGM) sensor experience
HbA1c <10.0%
Exclusion Criteria
Pregnancy
eGFR <40ml/min/1.73m2
History of diabetic ketoacidosis or severe hypoglycaemia in the last 3 months
Diabetic gastroparesis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time spent with sensor glucose 3.9–10.0 mmol/L using uploaded CGM data[1) Final 6 weeks of Stage 1 and Stage 2<br>2) During and 4 hours post-meal interventions eg. late meal-bolus; missed meal-bolus (specific to a particular intervention and aggregated)<br>]
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms differentiate FiASP from aspart in glucose regulation for type 1 diabetes?
How does FiASP compare to aspart in terms of hypoglycemia risk reduction within advanced closed-loop systems?
Which biomarkers correlate with improved glycemic control using FiASP in hybrid closed-loop therapy for type 1 diabetes?
What adverse events are associated with FiASP versus aspart in closed-loop insulin delivery systems?
How does FiASP's pharmacokinetic profile impact closed-loop system performance compared to traditional rapid-acting insulins in type 1 diabetes?