Metabolic Syndrome Observation on a Regional Basis

NCT ID: NCT00933010

Last Updated: 2010-10-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1600 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-10-31

Study Completion Date

2010-10-31

Brief Summary

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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.

Detailed Description

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Conditions

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Metabolic Syndrome

Study Design

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Observational Model Type

ECOLOGIC_OR_COMMUNITY

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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AstraZeneca

INDUSTRY

Sponsor Role lead

Responsible Party

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AstraZeneca

Principal Investigators

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Mario Mangrella

Role: STUDY_CHAIR

AstraZeneca S.p.A., R&D

Raffaele Sabia

Role: STUDY_DIRECTOR

AstraZeneca S.p.A., R&D

Locations

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Research

Foligno, , Italy

Site Status

Research Site

Perugia, , Italy

Site Status

Research Site

Terni, , Italy

Site Status

Countries

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Italy

Other Identifiers

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NIS-CIT-DUM-2008/1

Identifier Type: -

Identifier Source: org_study_id