drugset / Trial / NCT00151775

Assessment of Efficacy and Safety of Olmesartan Medoxomil in Children and Adolescent Patients With High Blood Pressure

NCT00151775

Phase 2/3 Completed 362 enrolled Daiichi Sankyo
RandomizedParallel-groupDouble-blindTreatment

Summary

This study assesses the efficacy and safety of olmesartan medoxomil in children ages 1-16 with high blood pressure. After a 5-week blinded treatment period of up to 5 weeks participants can continue to take olmesartan medoxomil (OM) for up to an additional 46 weeks.

Timeline

Start
2005-05
Primary completion
2008-09
Completion
2008-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Olmesartan medoxomil Unknown 0.3 mg/kg
Subject Olmesartan medoxomil Unknown 0.6 mg/kg
Subject Olmesartan medoxomil Unknown 2.5 mg
Subject Olmesartan medoxomil Unknown 10 mg
Subject Olmesartan medoxomil Unknown 40 mg

Indications