drugset / Trial / NCT00842075

Pramlintide in Adolescents With Type 1 Diabetes

NCT00842075

RandomizedParallel-groupOpen-labelHealth-services research

Summary

The investigators hypothesize that subcutaneous pramlintide as an adjunct to mealtime insulin immediately prior to meals can significantly reduce post-prandial glucose concentrations compared with mealtime insulin alone in children with type 1 diabetes. This is a 36 day, randomized, two-arm, open-label study with a treatment arm (taking pramlintide before all meals) and a control arm (diabetes regimen as usual).

Timeline

Start
2006-12
Primary completion
2009-12
Completion
2009-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Pramlintide Peptide 15 ug Subcutaneous