drugset / Trial / NCT02505971

Nadolol Versus Propranolol in Children With Infantile Hemangiomas

NCT02505971

Phase 3 Completed 74 enrolled The Hospital for Sick Children
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the efficacy and safety of oral propranolol versus nadolol in patients with Infantile Hemangiomas (IH) in a randomized, controlled, double-blinded study.

Timeline

Start
2015-09
Primary completion
2020-04
Completion
2020-06-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Nadolol Unknown 1.5 mg/kg
Comparator Nadolol Unknown 3 mg/kg
Comparator Propranolol Small molecule 1.5 mg/kg Oral
Comparator Propranolol Small molecule 3 mg/kg Oral

Indications