A Dose Ranging Study to Compare the Safety and Efficacy of Aliskiren in Patients With High Blood Pressure
Completed · Phase 3
Conditions studied: Hypertension
In brief
This is a study for people diagnosed with hypertension to compare 3 doses (75 mg, 150 mg, and 300 mg) of an experimental product, aliskiren in comparison to a placebo. Each patient is in the study for 8 weeks
Key facts
- Study ID
- NCT00260923
- Run by
- Novartis
- People needed
- 641
- Starts
- 2005-11-01
- Expected to finish
- 2006-11-01
- Last updated by the study team
- 2011-11-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male and female outpatients 18 years of age and older
- Patients who are eligible and able to participate in the study
You may not qualify if…
- Severe hypertension
- History or evidence of a secondary form of hypertension
- History of hypertensive encephalopathy or cerebrovascular accident.
- Other protocol-defined inclusion/exclusion criteria may apply
Where it is running
- Novartis Pharmaceuticals — East Hanover, New Jersey, United States
- Study site — Investigative Centers, Germany
Full record on ClinicalTrials.gov
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