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NCT00874952 Clinical Trial

Regional Observation of the Metabolic Syndrome

Metabolic Syndrome Clinical Trial

— ORSA  

Official title:
Regional Observation of the Metabolic Syndrome

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00874952
Other study ID # NIS-CIT-DUM-2007/1
Secondary ID
Status Completed
Phase N/A
First received April 2, 2009
Last updated February 16, 2010
Start date March 2009
Est. completion date February 2010

Study information
Verified date February 2010
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Observational

Clinical Trial Summary

The aim of the study, is to assess the prevalence of metabolic syndrome in Italy on a regional basis, defined according to National Cholesterol Education Program/Adult Treatment Panel III (NCEP/ATPIII) guidelines criteria.

Recruitment information / eligibility
Status Completed
Enrollment 1600
Est. completion date February 2010
Est. primary completion date February 2010
Accepts healthy volunteers No
Gender Both
Age group 40 Years to 74 Years
Eligibility Inclusion Criteria:

- Signed informed consent

- Laboratory analysis (lipidic profile and glycemia) performed in the last year

Exclusion Criteria:

- Subjects with serious or unstable medical or psychological conditions that, in the opinion of the investigator, would compromise the subject's successful participation in the study

- Pregnancy or breast feeding

- Patients enrolled in clinical studies which the aim is to evaluate the efficacy and/or tolerability of anti-hypertensive and/or lipid lowering drugs

Study Design

Observational Model: Ecologic or Community, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Locations
Country Name City State
Italy Research Site Torino

Sponsors (1)
Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Italy, 

Outcome
Type Measure Description Time frame Safety issue
Primary Prevalence of metabolic syndrome in primary care population At visit No
Primary Concomitant presence of other cardiovascular (CV) risk factors. At visit No
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