Effect of Valsartan on Lipid Subfractions in Hypertensive Patients With Metabolic Syndrome

NCT ID: NCT00394745

Last Updated: 2017-02-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

45 participants

Study Classification

INTERVENTIONAL

Study Start Date

2005-11-30

Study Completion Date

2007-06-30

Brief Summary

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The purpose of this study is to evaluate potential effects of valsartan on lipid subfractions and other parameters in lipid metabolism in patients with essential hypertension and metabolic syndrome.

Detailed Description

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Conditions

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Hypertension Metabolic Syndrome

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Valsartan

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Male or female outpatients \>= 18 years of age at Visit 1
* Hypertension (systolic blood pressure \>= 140 mmHg and \< 170 mmHg and/or diastolic blood pressure \>= 90 mmHg and \< 105 mmHg
* Elevated triglycerides
* Metabolic syndrome as defined by Adult Treatment Panel III criteria

Exclusion Criteria

* MSSBP \>= 170 mmHg and/or MSDBP \>= 105 mmHg at any time between Visit 1 and Visit 2
* Diabetes mellitus
* Patients treated with lipid lowering drugs in the last 6 weeks prior to Visit 1
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Novartis

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Novartis + 41 61 324 1111 Basel

Role: STUDY_DIRECTOR

Novartis Basel+ 41 61 324 1111

Locations

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Investigative Centers, , Germany

Site Status

Novartis

Basel, , Switzerland

Site Status

Countries

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Germany Switzerland

Other Identifiers

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CVAL489ADE25

Identifier Type: -

Identifier Source: org_study_id

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