Management of Cardiovascular Risk Factors

AstraZeneca1,492 enrolled

Overview

This practical experience should report a retrospective collection of data regarding cardiovascular risk factors of cardiovascular diseases. The goal is an evaluation of the development of the risk profile of cardiovascular patients with simultaneous treatment of hypertension and hyperlipidemia

Study Type

OBSERVATIONAL

Enrollment

1,492

Conditions

Cardiovascular Risk Factors Cardiovascular Diseases

Eligibility

Sex: ALLHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Patients received a anti-hypertension treatment in addition to cholesterol lowering treatment during the observation period * Patients received a cholesterol lowering treatment in addition to hypertension treatment during the observation period * Patients received during the observation time new cholesterol lowering and hypertension treatment Exclusion Criteria: * Patients received during the observation time only cholesterol lowering or only anti-hypertension treatment

Locations (36)

Outcomes

Primary Outcomes

The goal is an evaluation of the development of the risk profile of cardiovascular patients with simultaneous treatment of hypertension and hyperlipidemia.

Time frame: Inclusion visit, 6 to 9 months before inclusion visit and / or 12 to 15 months before inclusion visit

Data from ClinicalTrials.gov

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Research Site

Frick, Canton of Aargau, Switzerland

Research Site

Neuenhof, Canton of Aargau, Switzerland

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Riehen, Canton of Basel-City, Switzerland

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Thun, Canton of Bern, Switzerland

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Wynigen, Canton of Bern, Switzerland

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Geneva, Canton of Geneva, Switzerland

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Le Lignon, Canton of Geneva, Switzerland

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Meyrin, Canton of Geneva, Switzerland

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Schwyz, Canton of Schwyz, Switzerland

Research Site

Gerlafingen, Canton of Solothurn, Switzerland

...and 26 more locations