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OpenTrials
Completed

NCT Number: NCT00848380

Management of Cardiovascular Risk Factors

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

Completed

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Research Site, Arbedo, Canton Ticino, Switzerland

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. 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

Sponsors and collaborators

Lead sponsor

AstraZeneca

Industry

Registry information

Important dates

Study start
2009
Primary completion
2009
Study completion
2009
First posted
Feb 20, 2009
Registry last updated
Nov 16, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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