52 Week Trial of Liraglutide in Type 1 Diabetes
NCT01787916 · Completed
Last updated 2026-05-28This clinical trial tested the effects of the medication liraglutide in adults with type 1 diabetes over a 52-week period to observe changes in blood sugar control.
What this study is testing ClinicalTrials.gov NCT01787916 ↗
Description as written by the study sponsor.
To our knowledge, no trial has specifically studied the effect of liraglutide combined with a basal/bolus insulin regimen in type 1 diabetes in a cross-over, double-blind, unicentric model. Moreover, the potential impact of a glucagon-like peptide-1 agonist on measures of abdominal fat (assessed by CT scan), insulin sensitivity (assessed by the gold standard euglycemic-hyperinsulinemic clamp) and satiety sensations have not been evaluated in this population. Hypothesis Overweight participants with type 1 diabetes on liraglutide/insulin treatment will present improved glucose control with decreased HbA1c, decreased fasting and mean weekly glucose concentrations and glycemic excursions as well as increased insulin sensitivity compared to participants on placebo/insulin treatment. Participants with liraglutide/insulin treatment will also present improved endothelial function, lower body weight, central adipose tissue assessed by CT scan and higher satiety sensations assessed by visual analogue scales.
Treatments tested
- Liraglutide also known as Victoza Drug
Liraglutide will be compared to placebo for 24 weeks in a cross-over design
- Placebos Drug
placebo will be compared to liraglutide for 24 weeks in a cross-over design
| Main thing measured | Assessment of Changes in Glycemic Control by HbA1c. |
|---|---|
| Sponsor | CHU de Quebec-Universite Laval |
| Conditions studied | Type 1 Diabetes |
| GLP-1 drugs | liraglutide |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT01787916 ↗