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Antialbuminuric Effects of Valsartan and Lisinopril

Primary Purpose

Hypertension, Early Diabetic Nephropathy

Status
Terminated
Phase
Phase 4
Locations
Switzerland
Study Type
Interventional
Intervention
VALSARTAN, VALSARTAN PLUS HCTZ, LISINOPRIL, LISINOPRIL PLUS HCTZ
Sponsored by
Novartis
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypertension focused on measuring valsartan, lisinopril, albuminuria, diabetic nephropathy

Eligibility Criteria

40 Years - 75 Years (Adult, Older Adult)All Sexes

Inclusion Criteria: Male or female outpatients aged 40-75 years, Chronic nephropathy, as defined by a serum creatinine concentration of > 1.3 mg/dL or calculated glomerular filtration rate of > 30 mL/min/1.73 m2. Persistent albuminuria, as defined by urinary albumin excretion exceeding 20 mg/ 24 h but not > 1000 mg/ 24h. (for a minimum of three months). Hypertensive patients not adequately controlled with or without treatment (controlled: <130/80 mmHg). Written informed consent to participate in the study prior to any study procedures. Exclusion Criteria: Immediate need for renal replacement therapy. Treatment resistant oedema or nephrotic syndrome. Need for treatment with corticosteroids, non-steroidal antiinflammatory drugs, or immunosuppressive drugs. Albuminuria greater than 1000mg /24h and or less than 20mg/24h. Total cholesterol < 135mg/dl or not need for statins treatment. Renovascular hypertension Malignant hypertension MI, cerebrovascular accident within last year, severe peripheral vascular disease, CHF, chronic hepatic disease. Angiotensin converting enzyme inhibitors and angiotensin II receptors blockers within one month prior to randomization. A serum creatinine concentration >265 umol/L

Sites / Locations

  • Novartis Pharmaceuticals

Outcomes

Primary Outcome Measures

Change from baseline in urine albumin excretion rate from collected urine samples, after 16 and 20 weeks

Secondary Outcome Measures

Blood pressure less than 130/80 mmHg after 16 and 20 weeks of treatment
Change from baseline 48-hour ambulatory blood pressure, and blood pressure less than 130/80 mmHg after 16 and 20 weeks of treatment
Blood pressure less than 130/80 mmHg at night, measured by 48-hour ambulatory blood pressure monitoring, after 16 and 20 weeks of treatment
Change from baseline in size of left heart ventricle by electrocardiogram (ECG) after 20 weeks
Change from baseline in kidney function after 16 and 20 weeks

Full Information

First Posted
September 12, 2005
Last Updated
November 7, 2011
Sponsor
Novartis
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1. Study Identification

Unique Protocol Identification Number
NCT00171600
Brief Title
Antialbuminuric Effects of Valsartan and Lisinopril
Official Title
Comparative, Open Multicenter Trial Assessing the Effect on Albumin Excretion Rate of 320mg Valsartan (With or Without HCTZ) vs 40mg Lisinopril (With or Without HCTZ) on Hypertensive Patients With Diabetic and Non-diabetic Nephropathy and Albuminuria
Study Type
Interventional

2. Study Status

Record Verification Date
November 2011
Overall Recruitment Status
Terminated
Study Start Date
July 2005 (undefined)
Primary Completion Date
January 2007 (Actual)
Study Completion Date
January 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Novartis

4. Oversight

5. Study Description

Brief Summary
Title: Antialbuminuric effect of valsartan, lisinopril and valsartan versus lisinopril in non-diabetic and diabetic renal disease: a randomized (3:3:1), open label, parallel group, 20 weeks follow-up. Objective: To evaluate the antialbuminuric effect of high doses of valsartan vs lisinopril vs combo treatment in non-diabetic and diabetic patients. Hypothesis: Combo treatment reduces microalbuminuria and the albumin/creatinine ratio more than monotherapies.. Design: Multicentric, randomized, open label, parallel group, active controlled. Dose / regimen: Valsartan 320 vs Lisinopril 40 vs Valsartan/lisinopril 160/20 Primary Endpoint: Antialbuminuric effect of valsartan 320 mg, lisinopril and valsartan versus lisinopril 40 mg in non-diabetic and diabetic renal disease following 5 months of follow-up. Description % of change in albuminuria from baseline at 20 weeks. Secondary Endpoint : To investigate the effect of 5 months treatment with valsartan,lisinopril and valsartan versus lisinopril in GFR (Cl creatinine), also to investigate the effect of 5 months treatment with valsartan, lisinopril and valsartan plus lisinopril on blood pressure and the effect on left ventricular mass index using electrocardiogram and Cornell-Sokolow method.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Early Diabetic Nephropathy
Keywords
valsartan, lisinopril, albuminuria, diabetic nephropathy

7. Study Design

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

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
VALSARTAN, VALSARTAN PLUS HCTZ, LISINOPRIL, LISINOPRIL PLUS HCTZ
Primary Outcome Measure Information:
Title
Change from baseline in urine albumin excretion rate from collected urine samples, after 16 and 20 weeks
Secondary Outcome Measure Information:
Title
Blood pressure less than 130/80 mmHg after 16 and 20 weeks of treatment
Title
Change from baseline 48-hour ambulatory blood pressure, and blood pressure less than 130/80 mmHg after 16 and 20 weeks of treatment
Title
Blood pressure less than 130/80 mmHg at night, measured by 48-hour ambulatory blood pressure monitoring, after 16 and 20 weeks of treatment
Title
Change from baseline in size of left heart ventricle by electrocardiogram (ECG) after 20 weeks
Title
Change from baseline in kidney function after 16 and 20 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Eligibility Criteria
Inclusion Criteria: Male or female outpatients aged 40-75 years, Chronic nephropathy, as defined by a serum creatinine concentration of > 1.3 mg/dL or calculated glomerular filtration rate of > 30 mL/min/1.73 m2. Persistent albuminuria, as defined by urinary albumin excretion exceeding 20 mg/ 24 h but not > 1000 mg/ 24h. (for a minimum of three months). Hypertensive patients not adequately controlled with or without treatment (controlled: <130/80 mmHg). Written informed consent to participate in the study prior to any study procedures. Exclusion Criteria: Immediate need for renal replacement therapy. Treatment resistant oedema or nephrotic syndrome. Need for treatment with corticosteroids, non-steroidal antiinflammatory drugs, or immunosuppressive drugs. Albuminuria greater than 1000mg /24h and or less than 20mg/24h. Total cholesterol < 135mg/dl or not need for statins treatment. Renovascular hypertension Malignant hypertension MI, cerebrovascular accident within last year, severe peripheral vascular disease, CHF, chronic hepatic disease. Angiotensin converting enzyme inhibitors and angiotensin II receptors blockers within one month prior to randomization. A serum creatinine concentration >265 umol/L
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Novartis Pharmaceuticals
Organizational Affiliation
Novartis Pharmaceuticals
Official's Role
Study Director
Facility Information:
Facility Name
Novartis Pharmaceuticals
City
Basel
Country
Switzerland

12. IPD Sharing Statement

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Antialbuminuric Effects of Valsartan and Lisinopril

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