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Efficacy and Safety of Valsartan/Amlodipine Combination in Patients With Severe Hypertension

Phase 3
Completed
Conditions
Hypertension
Registration Number
NCT00171535
Lead Sponsor
Novartis
Brief Summary

This study will assess the effectiveness and safety of different combination antihypertensive treatments in patients with severe hypertension

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
130
Inclusion Criteria
  • Patients with severe hypertension
Exclusion Criteria
  • History of stroke, myocardial infarction, heart failure, chest pain, abnormal heart rhythm
  • Liver, kidney, or pancreas disease
  • Insulin dependent diabetes
  • Allergy to certain medications used to treat high blood pressure

Other protocol-defined inclusion/exclusion criteria may apply.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Adverse events and serious adverse events at each study visit for 6 weeks
Secondary Outcome Measures
NameTimeMethod
Sitting and standing blood pressure measurements after 6 weeks
Laboratory test data after 6 weeks
Vital signs at each study visit for 6 weeks

Trial Locations

Locations (1)

Novartis Pharmaceuticals

🇺🇸

East Hanover, New Jersey, United States

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