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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00848380
Other study ID # NIS-CCH-DUM-2008/2
Secondary ID
Status Completed
Phase N/A
First received February 19, 2009
Last updated November 15, 2010
Start date February 2009
Est. completion date December 2009

Study information

Verified date November 2010
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial Summary

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


Recruitment information / eligibility

Status Completed
Enrollment 1492
Est. completion date December 2009
Est. primary completion date December 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility 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

Study Design

Observational Model: Case Control, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Switzerland Research Site Affoltern am Albis ZH
Switzerland Research Site Andeer GR
Switzerland Research Site Arbedo TI
Switzerland Research Site Bassins VD
Switzerland Research Site Bellinzona TI
Switzerland Research Site Claro TI
Switzerland Research Site Coldrerio TI
Switzerland Research Site Feldmeilen ZH
Switzerland Research Site Frick AG
Switzerland Research Site Geneve GE
Switzerland Research Site Gerlafingen SO
Switzerland Research Site Gland VD
Switzerland Research Site Herrliberg ZH
Switzerland Research Site Ilanz GR
Switzerland Research Site Langnau am Albis ZH
Switzerland Research Site Lausanne VD
Switzerland Research Site Le Lignon GE
Switzerland Research Site Locarno TI
Switzerland Research Site Lohn SO SO
Switzerland Research Site Lugano TI
Switzerland Research Site Meyrin GE
Switzerland Research Site Montreux VD
Switzerland Research Site Muralto TI
Switzerland Research Site Neuenhof AG
Switzerland Research Site Nyon VD
Switzerland Research Site Richterswil ZH
Switzerland Research Site Riehen BS
Switzerland Research Site Rorschach SG
Switzerland Research Site Ruti ZH ZH
Switzerland Research Site Schwyz SZ
Switzerland Research Site St. Gallen SG
Switzerland Research Site Thun BE
Switzerland Research Site Wynigen BE
Switzerland Research Site Zuchwil SO
Switzerland Research Site Zug ZG
Switzerland Research Site Zurich ZH

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary The goal is an evaluation of the development of the risk profile of cardiovascular patients with simultaneous treatment of hypertension and hyperlipidemia. Inclusion visit, 6 to 9 months before inclusion visit and / or 12 to 15 months before inclusion visit No
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