drugset / Trial / NCT04414579

The Efficacy and Safety of Faster Insulin Aspart (Fiasp®) Compared to Conventional Insulin Aspart (NovoLog®) as Correction Bolus

NCT04414579 ↗

Phase 4 Unknown 45 enrolled Mountain Diabetes and Endocrine Center
RandomizedCrossoverOpen-labelTreatment

Summary

The purpose of this investigator-initiated trial is to compare the efficacy in terms of time to recovery from hyperglycemia as measured by time to arrest of hyperglycemic excursion ("glucose plateau point", primary endpoint) and return to premeal glucose target if feasible (secondary endpoint) between Fiasp and conventional insulin aspart when used as a correction bolus. These endpoints will be determined by CGM (Dexcom) from data exported from the Dexcom Clarity program.

Timeline

Start
2019-03-27
Primary completion
2021-03
Completion
2021-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Conventional Insulin Aspart Unknown — Subcutaneous
Comparator Faster Insulin Aspart Unknown — —