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Efficacy and Safety of Aliskiren and Atenolol in Adults (>18) With Mild to Moderate Hypertension

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Novartis

Status and phase

Completed
Phase 3

Conditions

Hypertension

Treatments

Drug: Aliskiren

Study type

Interventional

Funder types

Industry

Identifiers

NCT00262236
CSPP100A2304

Details and patient eligibility

About

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.

Enrollment

693 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Outpatients 18 years of age and older.
  2. 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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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