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NCT00933010 Clinical Trial

Metabolic Syndrome Observation on a Regional Basis

Metabolic Syndrome Clinical Trial

— ORSA Umbria  

Official title:
Osservatorio Regionale Sulla Sindrome metabolicA

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00933010
Other study ID # NIS-CIT-DUM-2008/1
Secondary ID
Status Completed
Phase N/A
First received July 2, 2009
Last updated October 12, 2010
Start date October 2009
Est. completion date October 2010

Study information
Verified date October 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 NCEP/ATPIII Guidelines criteria.

Recruitment information / eligibility
Status Completed
Enrollment 1600
Est. completion date October 2010
Est. primary completion date October 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Patient aged between 18 and 75 years

- Signed Informed consent

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

Exclusion Criteria:

- 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

- 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

Study Design

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

Related Conditions & MeSH terms

Locations
Country Name City State
Italy Research Foligno
Italy Research Site Perugia
Italy Research Site Terni

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 July 2009 - March 2010 No
Primary Concomitant presence of other CV risk factors July 2009 - March 2010 No
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