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The Impact of Two Different Insulin Dose Calculation on Postprandial Glycemia After Mixed Meal.

NCT04124302 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 76

Last updated 2025-11-18

No results posted yet for this study

Summary

The aim of the study is to compare the impact of two different insulin dose calculation on postprandial glycemia after mixed meal in children with type 1 diabetes mellitus.

Conditions

  • Diabetes Mellitus, Type 1

Interventions

DRUG

Insulin Glulisine

A kind of bolus insulin will be insulin glulisine if participant used insulin glulisine before entering the trial.

DRUG

Insulin Aspart

A kind of bolus insulin will be insulin aspart if participant used insulin aspart before entering the trial.

DRUG

Insulin Lispro

A kind of bolus insulin will be insulin lispro if participant used insulin lispro before entering the trial.

Sponsors & Collaborators

  • Medical University of Warsaw

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
10 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-10-01
Primary Completion
2024-03-27
Completion
2024-12-31

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04124302 on ClinicalTrials.gov