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Metabolic Syndrome Observation on a Regional Basis (ORSA Umbria)

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Metabolic Syndrome

Study type

Observational

Funder types

Industry

Identifiers

NCT00933010
NIS-CIT-DUM-2008/1

Details and patient eligibility

About

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.

Enrollment

1,600 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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