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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00689455
Other study ID # NIS-CIT-DUM-2008/2
Secondary ID
Status Completed
Phase N/A
First received May 29, 2008
Last updated December 2, 2010
Start date October 2007
Est. completion date December 2008

Study information

Verified date December 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 1574
Est. completion date December 2008
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- lipid profile in the last year

- Signed informed consent

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

- Subject who are unwilling or unable to provide the informed consent

Study Design

Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Italy Research Site Rieti
Italy Research Site ROme
Italy Research Site Viterbo

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
Secondary Concomitant presence of other CV risk factors. At Visit
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