Status:

COMPLETED

A Dose Ranging Study to Compare the Safety and Efficacy of Aliskiren 150mg, 300mg, and 600mg to Placebo in Patients With High Blood Pressure.

Lead Sponsor:

Novartis

Conditions:

Hypertension

Eligibility:

All Genders

18+ years

Phase:

PHASE3

Brief Summary

Evaluate the blood pressure lowering effect of aliskiren 150mg, 300mg and 600mg compared to placebo in patients with essential hypertension

Eligibility Criteria

Inclusion

  • Inclusion Criteria
  • Patients with essential hypertension
  • Patients who are eligible and able to participate in the study
  • Exclusion Criteria
  • Severe hypertension
  • History or evidence of a secondary form of hypertension
  • History of Hypertensive encephalopathy or cerebrovascular accident.
  • Other protocol-defined exclusion criteria may apply.

Exclusion

    Key Trial Info

    Start Date :

    November 1 2004

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    June 1 2005

    Estimated Enrollment :

    671 Patients enrolled

    Trial Details

    Trial ID

    NCT00219128

    Start Date

    November 1 2004

    End Date

    June 1 2005

    Last Update

    November 8 2011

    Active Locations (1)

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    Novartis Pharmaceuticals

    East Hanover, New Jersey, United States, 07936