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Valsartan in Cardiovascular Disease With Renal Dysfunction (The V-CARD) Study

Primary Purpose

Hypertension

Status
Terminated
Phase
Phase 4
Locations
Japan
Study Type
Interventional
Intervention
valsartan
Sponsored by
Kumamoto University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hypertension focused on measuring Cardiorenal syndrome, Renal dysfunction, Cardiovascular events, Valsartan

Eligibility Criteria

30 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria (all required): Systolic blood pressure (SBP) >/= 140 and/or diastolic blood pressure (DBP) >/= 90 (untreated hypertension cases); or SBP>/=130 and/or DBP>/=80 (treated hypertension cases) Patients with coronary artery disease (more than 50% stenosis on coronary angiography [CAG], coronary computed tomography [CT] or coronary magnetic resonance angiography [MRA]; coronary spasm; or history of percutaneous coronary intervention [PCI]);Unstable angina patient Creatinine clearance between 30.0 and 89.9 ml/min Exclusion Criteria (at least one of following): Reduced left ventricular (LV) function (ejection fraction [EF] equal to or less than 40%) Hyperpotassemia (serum potassium equal to or more than 5.5 mEq/l) Rapid progressive glomerular nephritis Nephrotic syndrome Renal artery stenosis Uncontrolled diabetes (HbA1c equal to or more than 9.0%) History of allergy to valsartan Pregnant women

Sites / Locations

  • Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University
  • Department of Cardiovascular Medicine, Kumamoto University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Valsartan 40mg

Valsartan 160mg

Arm Description

Standard Dose valsartan

High Dose valsartan

Outcomes

Primary Outcome Measures

Cardiovascular events
End-stage renal dysfunction
50% reduction of creatinine clearance

Secondary Outcome Measures

% FS and E/A ratio
Specific biochemical markers for cardiac or renal function
% changes of creatinine clearance
1/(serum Cr)
Serum K
HbA1c
U-prot/U-Cr
Adverse drug effects
New onset Atrial Fibrillation

Full Information

First Posted
August 31, 2005
Last Updated
February 25, 2016
Sponsor
Kumamoto University
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1. Study Identification

Unique Protocol Identification Number
NCT00140790
Brief Title
Valsartan in Cardiovascular Disease With Renal Dysfunction (The V-CARD) Study
Official Title
Effects of Valsartan on Cardiovascular Events in Patients With Renal Dysfunction
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Terminated
Why Stopped
The number of actual events was extremely low. We extended the study period, but it was still not enough. Also, many patients were loss of follow up.
Study Start Date
August 2006 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
March 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kumamoto University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to investigate if an angiotensin II receptor blocker, valsartan 160 mg/day is more effective to reduce the incidence of cardiovascular events as compared to 40 mg/day in patients with moderate renal dysfunction.
Detailed Description
It is well known that patients with renal dysfunction have a poor prognosis concerning cardiovascular diseases. That is called "cardiorenal syndrome". It was reported that valsartan was effective in reducing the urine albumin extraction rate in patients with hyper- or normotension. We hypothesized that valsartan was more effective to prevent cardiovascular events by the intermediary of improving renal function. The primary endpoints are: cardiovascular events (cardiac death, non-fatal myocardial infarction, unstable angina requiring rehospitalization, congestive heart failure requiring rehospitalization, revascularization procedures including coronary angioplasty or coronary artery bypass grafting;Stroke or transient ischaemic attack, dissociation aneurysm of the aorta needing hospitalisation;Lower limbs artery obstruction needing hospitalisation . end-stage renal dysfunction (introduction of hemodialysis or kidney transplantation) 50% reduction of creatinine clearance The secondary endpoints are: systolic and diastolic function of the left ventricle estimated by echocardiography (% FS and E/A ratio) specific biochemical markers for cardiac or renal function (urine microalbumin, plasma B-type natriuretic peptide, plasma type 1 plasminogen activator inhibitor, plasma cystatin C) % changes of creatinine clearance between start and end of the study period transition of 1/(serum Cr) in patients whose u-prot/u-Cr is equal to or more than 1.0 transition of serum K HbA1c New onset Atrial Fibrillation New onset Diabetes

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension
Keywords
Cardiorenal syndrome, Renal dysfunction, Cardiovascular events, Valsartan

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1000 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Valsartan 40mg
Arm Type
Active Comparator
Arm Description
Standard Dose valsartan
Arm Title
Valsartan 160mg
Arm Type
Active Comparator
Arm Description
High Dose valsartan
Intervention Type
Drug
Intervention Name(s)
valsartan
Intervention Description
valsartan 40 or 160 (80) mg per day
Primary Outcome Measure Information:
Title
Cardiovascular events
Time Frame
2 years
Title
End-stage renal dysfunction
Time Frame
2 years
Title
50% reduction of creatinine clearance
Time Frame
2 years
Secondary Outcome Measure Information:
Title
% FS and E/A ratio
Time Frame
2 years
Title
Specific biochemical markers for cardiac or renal function
Time Frame
6 months and 1 year and 2 years
Title
% changes of creatinine clearance
Time Frame
2 years
Title
1/(serum Cr)
Time Frame
2 years
Title
Serum K
Time Frame
2 years
Title
HbA1c
Time Frame
2 years
Title
U-prot/U-Cr
Time Frame
2 years
Title
Adverse drug effects
Time Frame
2 years
Title
New onset Atrial Fibrillation
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria (all required): Systolic blood pressure (SBP) >/= 140 and/or diastolic blood pressure (DBP) >/= 90 (untreated hypertension cases); or SBP>/=130 and/or DBP>/=80 (treated hypertension cases) Patients with coronary artery disease (more than 50% stenosis on coronary angiography [CAG], coronary computed tomography [CT] or coronary magnetic resonance angiography [MRA]; coronary spasm; or history of percutaneous coronary intervention [PCI]);Unstable angina patient Creatinine clearance between 30.0 and 89.9 ml/min Exclusion Criteria (at least one of following): Reduced left ventricular (LV) function (ejection fraction [EF] equal to or less than 40%) Hyperpotassemia (serum potassium equal to or more than 5.5 mEq/l) Rapid progressive glomerular nephritis Nephrotic syndrome Renal artery stenosis Uncontrolled diabetes (HbA1c equal to or more than 9.0%) History of allergy to valsartan Pregnant women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hisao Ogawa, MD, PhD
Organizational Affiliation
Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University
City
Kumamoto
ZIP/Postal Code
860-8556
Country
Japan
Facility Name
Department of Cardiovascular Medicine, Kumamoto University Hospital
City
Kumamoto
ZIP/Postal Code
860-8556
Country
Japan

12. IPD Sharing Statement

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Valsartan in Cardiovascular Disease With Renal Dysfunction (The V-CARD) Study

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