Valsartan Optimal Therapy Against Elevated Home Blood Pressure Research（VOYAGER）Study

NCT ID: NCT00460213

Last Updated: 2013-12-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 103 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-07-31
• Study Completion Date: 2013-11-30

Brief Summary

The purpose of this study is to compare improvement percentage of urinary albumin excretion between valsartan 80 mg- and valsartan 160 mg-based therapy in patient with morning hypertension.

Detailed Description

The cardiovascular diseases such as stroke and myocardial infarction consist 50% of the cause of death in Japanese population. Numerous mega trials have shown that strict anti-hypertensive therapy could reduce cardiovascular morbidity and mortality in hypertensive patients.

It is reported, however, over 50% hypertensive patients have not been controlled below therapeutic target blood pressure that the JSH2004 guideline recommends.

Recently use of Angiotensin II receptor blockers (ARBs) is increasing progressively for their pharmacological action on organ protection as well as potent reduction in blood pressure. However, usual dosage of ARB in Japan is almost half of that in the mega trials executed in Europe and America. Lower dosage compared to western countries might be a reason why cardiovascular events are not fully reduced in Japan.

Valsartan optimal therapy against elevated home blood pressure research (VOYAGER) study will be a multi-center, open-label, randomized, active-controlled study to evaluate the following; improvement percentage of urinary albumin exception, home blood pressure, hospital blood pressure, incidence of stroke, cardiovascular disease, and microangiopathy with valsartan 80 mg- or valsartan 160 mg based therapy in patients with elevated morning home blood pressure.

Conditions

Hypertension

Keywords

home blood pressure

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Valsartan

Group Type: EXPERIMENTAL

Valsartan 80mg daily

Intervention Type: DRUG

Valsartan 160mg daily

Intervention Type: DRUG

Interventions

Valsartan 80mg daily

Intervention Type: DRUG

Valsartan 160mg daily

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Outpatients aged over 20 years and less than 80 years, regardless of sex.
• Patients with stable seated morning home blood pressure of over 135 mmHg and/or diastolic blood pressure of over 85 mmHg within 1 to 2 weeks.
• Patients who are on therapy with conventional dosage of ARB.

Exclusion Criteria

• Patients who are difficult to measure home blood pressure.
• Patients with secondary hypertension or malignant hypertension.
• Patients with seated systolic blood pressure of over 200 mmHg.
• Patients with seated diastolic blood pressure of over 120 mmHg.
• Patients with a history of cerebrovascular disorder or myocardial infarction or heart failure within 6 months prior to enrolment in the study.
• Patients with atrial fibrillation, atrial flutter, or serious arrhythmia.
• Patients with renal dysfunction with serum creatinine level of over 2 mg/dL.
• Patients with serious liver dysfunction.
• Patient with HbA1C of over 8 percent.
• Patient with positive albuminuria by dip and read stick test.
• Patient treated with any angiotensin converting enzyme inhibitor
• Pregnant women
• Patients with a history of hypersensitivity to valsartan.
• Other patients who are judged to be inappropriate for the study by the investigator or sub-investigator.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Kitakyushu-Tsuyazaki Hospital

OTHER

Sponsor Role: lead

Responsible Party

Koshiro Fukiyama

Honorary Director

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Koshiro Fukiyama, MD

Role: STUDY_CHAIR

Japan Seamen's Relief Association Moji Hospital

Locations

Koshiro Fukiyama

Kitakyushu, Fukuoka, Japan

Countries

Japan

Other Identifiers

ISRCTN1150

Identifier Type: -

Identifier Source: secondary_id

KIT-061003-1

Identifier Type: -

Identifier Source: org_study_id