NCT Number: NCT00262236
Efficacy and Safety of Aliskiren and Atenolol in Adults (>18) With Mild to Moderate Hypertension
This is a study for people diagnosed with hypertension to compare the safety and effectiveness of aliskiren alone and in combination with atenolol. Each patient will be in the study for 12 weeks.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
Investigative Centers, Germany
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Outpatients 18 years of age and older.
- Patients with essential hypertension.
Exclusion criteria
Severe hypertension, Current diagnosis of heart failure, History or evidence of a secondary form of hypertension, Participation in any investigational drug study within one month of planned participation,
Other protocol-defined inclusion/exclusion criteria may apply
Treatment and study plan
Primary outcomes
-
Change from baseline in diastolic blood pressure after 12 weeks
Secondary outcomes
-
Change from baseline in systolic blood pressure after 12 weeks
-
Diastolic blood pressure < 90 mmHg or a reduction of > 10 mmHg after 12 weeks
-
Blood pressure of < 140/90 mmHg after 12 weeks
Sponsors and collaborators
Lead sponsor
Novartis
Industry
Registry information
Official study title
A Twelve-week, Randomized, Double-blind, Parallel-group, Multicenter, Dose Escalation Study to Evaluate the Efficacy and Safety of Aliskiren Administered Alone and in Combination With Atenolol in Patients With Essential Hypertension
Important dates
- Study start
- 2005
- Primary completion
- 2006
- Study completion
- 2006
- First posted
- Dec 6, 2005
- Registry last updated
- Nov 18, 2016
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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