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Sponsored by: |
Novartis |
Information provided by: | Novartis |
ClinicalTrials.gov Identifier: | NCT00219193 |
To evaluate the blood pressure lowering effect and safety of the triple combination aliskiren / valsartan / HCTZ (300/320/25 mg) in patients with essential hypertension not adequately responsive to HCTZ 25 mg
Condition | Intervention | Phase |
Hypertension |
Drug: aliskiren |
Phase III |
MedlinePlus related topics: | High Blood Pressure |
Drug Information available for: | Valsartan Aliskiren |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study |
Official Title: | An Eight Week, Multicenter Study to Evaluate Efficacy and Safety of the Triple Combo of Aliskiren /Valsartan/HCTZ (300/320/25 mg), Compared to the Double Combos of Aliskiren/HCTZ (300/25 mg) or Valsartan/HCTZ (320/25 mg) in Patients With Essential Hypertension Not Adequately Responsive to HCTZ 25 mg |
Estimated Enrollment: | 624 |
Study Start Date: | October 2005 |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria
Exclusion Criteria
Other protocol-defined exclusion criteria may apply.
United States, New Jersey | |||||
Novartis Pharmaceuticals | |||||
East Hanover, New Jersey, United States, 07936 | |||||
Germany | |||||
Investigative Centers, Germany |
Novartis |
Study Director: | Novartis Pharmaceuticals | Novartis Pharmaceuticals |
Study ID Numbers: | CSPP100A2331 |
First Received: | September 12, 2005 |
Last Updated: | February 13, 2007 |
ClinicalTrials.gov Identifier: | NCT00219193 |
Health Authority: | United States: Food and Drug Administration |
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