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| Sponsor: | Novartis |
|---|---|
| Information provided by: | Novartis |
| ClinicalTrials.gov Identifier: | NCT00426478 |
Purpose
A double-blind, active-controlled, randomized trial to compare Valsartan plus Hydrochlorothiazide 80mg/12.5mg and Amlodipine 5 mg.
Study design: 2 weeks washout, 8 weeks treatment period.
| Condition | Intervention | Phase |
|---|---|---|
|
Hypertension |
Drug: Valsartan plus Hydrochlorothiazide (80mg/12.5mg) Drug: Amlodipine (5mg) |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study |
| Official Title: | The Comparison of the Antihypertensive Efficacy and Tolerability Between Valsartan Plus Hydrochlorothiazide 80mg/12.5mg and Amlodipine 5mg in the Essential Hypertensive Patients |
| Estimated Enrollment: | 80 |
| Study Start Date: | November 2006 |
| Study Completion Date: | September 2007 |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Other protocol-defined inclusion/exclusion criteria may apply
Contacts and Locations
More Information
| Study ID Numbers: | CVAH631BTW02 |
| Study First Received: | January 23, 2007 |
| Last Updated: | August 20, 2008 |
| ClinicalTrials.gov Identifier: | NCT00426478 History of Changes |
| Health Authority: | Taiwan: Department of Health |
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AMPM, SBP, DBP, Valsartan plus Hydrochlorothiazide, Amlodipine, high blood pressure |
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Vasodilator Agents Molecular Mechanisms of Pharmacological Action Diuretics Physiological Effects of Drugs Sodium Chloride Symporter Inhibitors Vascular Diseases Calcium Channel Blockers Cardiovascular Agents Antihypertensive Agents |
Hydrochlorothiazide Pharmacologic Actions Amlodipine Membrane Transport Modulators Natriuretic Agents Therapeutic Uses Cardiovascular Diseases Valsartan Hypertension |