valsartan
DrugWeight stratified dosages given by mouth, once daily, of valsartan 80/160/320 mg.
NCT Number: NCT00433836
The purpose of this 12-week active controlled trial is to evaluate the safety and efficacy of valsartan 80/160/320 mg (weight stratified) compared with enalapril 10/20/40 mg (weight stratified) on sitting systolic blood pressure (SSBP) in 6 - 17 year old children with hypertension (SSBP ≥ 95th percentile for age gender and height).
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Notify Me6 year–17 year
All sexes
Interventional
Phase 3
Sites in Belgium, Belgium
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other protocol-defined inclusion/exclusion criteria may apply
Weight stratified dosages given by mouth, once daily, of valsartan 80/160/320 mg.
Weight stratified dosages given by mouth, once daily, of enalapril 10/20/40 mg.
Time frame: Baseline and Week 12
Mean sitting systolic blood pressure (MSSBP) change after 12 weeks of treatment measured by office blood pressure measurement.
Time frame: Baseline and Week 12
The change from baseline in mean sitting diastolic blood pressure (MSDBP) after 12 weeks of treatment as measured by office blood pressure.
Time frame: at week 12
The percentage of children whose MSSBP decreased to <95th percentile for age, gender, and height on valsartan vs. enalapril monotherapy at week 12.
Time frame: Baseline and Week 8
The effect of valsartan and enalapril between baseline and visit 6 on 24-hour mean ambulatory systolic and diastolic blood pressure (ASBP, ADBP) in a subset of patients.
Novartis Pharmaceuticals
Industry
A Multicenter, Randomized, Double-blind, Parallel-group, Evaluation of 12 Weeks of Valsartan Compared to Enalapril on Sitting Systolic Blood Pressure in Children 6 to 17 Years of Age With Hypertension
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