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A Morbidity-Mortality and Remodeling Study With Valsartan
This study is ongoing, but not recruiting participants.
Sponsored by: Jikei University School of Medicine
Information provided by: Jikei University School of Medicine
ClinicalTrials.gov Identifier: NCT00133328
  Purpose

The JIKEI HEART Study has been designed to investigate whether concomitant treatment with valsartan, an angiotensin II receptor blocker (ARB), in addition to conventional treatment, will improve the prognosis of 3000 Japanese patients with cardiovascular diseases.


Condition Intervention Phase
Hypertension
Ischemic Heart Disease
Congestive Heart Failure
Drug: valsartan
Phase IV

MedlinePlus related topics: Angina Heart Attack Heart Diseases Heart Failure High Blood Pressure
Drug Information available for: Valsartan
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title: A Morbi-Mortality and Remodeling Study With Valsartan in Patients With Hypertension and Cardiovascular Disease

Further study details as provided by Jikei University School of Medicine:

Primary Outcome Measures:
  • stroke
  • new or recurrent transient ischemic attack
  • new or recurrent acute myocardial infarction
  • new occurrence or exacerbation of heart failure
  • new occurrence or exacerbation angina pectoris
  • dissecting aneurysm of the aorta
  • lower limb arterial obstruction
  • transition to dialysis
  • doubling of plasma creatinine (Cr) levels

Secondary Outcome Measures:
  • death from any cause
  • left ventricular hypertrophy
  • changes in ECG
  • proteinuria
  • B-type natriuretic peptide (BNP)
  • heart failure symptoms
  • heart failure syndrome (edema, rales on auscultation)
  • blood pressure and heart rate

Estimated Enrollment: 3000
Study Start Date: January 2002
Estimated Study Completion Date: November 2005
Detailed Description:

Several recent clinical trials have demonstrated that angiotensin II receptor blockers (ARBs) have cardiovascular as well as renal protective effects. However, it is a problem that the number of Asian patients is very little in these trials. The researchers examine the treatment meaning by ARB about the prognosis of the patient who amalgamates either among high blood pressure, the ischemic heart disease, and congestive heart failures.

  Eligibility

Ages Eligible for Study:   20 Years to 79 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Clinical diagnosis of hypertension, ischemic heart disease and congestive heart failure

Exclusion Criteria:

  • Pregnancy
  • Severe renal damage
  • Severe liver damage
  • Acute myocardial infarction
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00133328

Locations
Japan
The Jikei University School of Medicine
Tokyo, Japan, 105-8461
Sponsors and Collaborators
Jikei University School of Medicine
Investigators
Study Chair: Seibu Mochizuki, MD., PhD The Jikei University School of Medicine
  More Information

Publications of Results:
Publications indexed to this study:
Study ID Numbers: JHS2002
Study First Received: August 22, 2005
Last Updated: October 27, 2005
ClinicalTrials.gov Identifier: NCT00133328  
Health Authority: Japan: Ministry of Health, Labor and Welfare

Keywords provided by Jikei University School of Medicine:
stroke
myocardial infarction
angina
renal damage

Study placed in the following topic categories:
Heart Failure
Heart Diseases
Cerebral Infarction
Myocardial Ischemia
Stroke
Vascular Diseases
Angina Pectoris
Ischemia
Infarction
Myocardial Infarction
Valsartan
Hypertension

Additional relevant MeSH terms:
Therapeutic Uses
Cardiovascular Diseases
Cardiovascular Agents
Antihypertensive Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 14, 2009