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OpenTrials
Completed

NCT Number: NCT00426478

Safety and Efficacy of Valsartan Plus Hydrochlorothiazide and Amlodipine in Hypertensive Patients

A double-blind, active-controlled, randomized trial to compare Valsartan plus Hydrochlorothiazide 80mg/12.5mg and Amlodipine 5 mg.

Study design: 2 weeks washout, 8 weeks treatment period.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

National Taiwan University

Taipei, R.o.c, 100, Taiwan

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female or male patient with age ≧ 18 years old.
  • Patient with mild to moderate uncomplicated essential hypertension, and the blood pressure not adequately controlled on existing antihypertensive treatment.
  • Patient with sitting systolic blood pressure (sSBP)/ sitting diastolic blood pressure (sDBP) ≦ 180/110 mmHg at screening visit.
  • For non-diabetic patient, sitting systolic blood pressure (sSBP) ≧ 140 mmHg or sitting diastolic blood pressure (sDBP) ≧ 90 mmHg at baseline visit; for diabetic patient, sitting systolic blood pressure (sSBP) ≧ 130 mmHg or sitting diastolic blood pressure (sDBP) ≧ 80 mmHg at baseline visit.
  • Patient or his/her legally acceptable representative has signed and dated the informed consent form.

Exclusion criteria

  • Known or suspected secondary hypertension.
  • sSBP > 180 mmHg or sDBP > 110 mmHg at baseline visit.
  • Patients taking more than two anti-hypertensive medications at the screening visit. (Fixed-dose combinations of two or more antihypertensive therapies will be counted as two or more antihypertensive medications.)
  • Known NYHA functional class Chronic Heart Failure (CHF) III and IV.
  • With a history of myocardial infarction, transient ischemic attack or cerebrovascular accident within the preceding 6 months, clinically significant valvular heart disease, or hepatic and/or renal dysfunction as defined by the following laboratory parameters
  • SGPT (ALT) or SGOT (AST) > two times upper the limit of normal range
  • Serum creatinine > 2.3 mg/dl or creatinine clearance < 30 ml/min

Other protocol-defined inclusion/exclusion criteria may apply

Treatment and study plan

Valsartan plus Hydrochlorothiazide (80mg/12.5mg)

Drug

Amlodipine (5mg)

Drug

Primary outcomes

  1. Change from baseline in mean sitting systolic blood pressure (msSBP) after 8 weeks treatment

Secondary outcomes

  1. Change from baseline in mean sitting diastolic blood pressure (msDBP) after 8 weeks treatment

  2. Change from baseline in Ambulatory Blood Pressure Measurement (ABPM) parameters after 8 weeks treatment

Sponsors and collaborators

Lead sponsor

Novartis

Industry

Registry information

Official study title

The Comparison of the Antihypertensive Efficacy and Tolerability Between Valsartan Plus Hydrochlorothiazide 80mg/12.5mg and Amlodipine 5mg in the Essential Hypertensive Patients

Important dates

Study start
2006
Study completion
2007
First posted
Jan 24, 2007
Registry last updated
Aug 22, 2008

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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