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OpenTrials
Completed

NCT Number: NCT00933010

Metabolic Syndrome Observation on a Regional Basis

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.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Research, Foligno, Italy

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Prevalence of Metabolic Syndrome in Primary Care Population

    Time frame: July 2009 - March 2010

  2. Concomitant presence of other CV risk factors

    Time frame: July 2009 - March 2010

Sponsors and collaborators

Lead sponsor

AstraZeneca

Industry

Registry information

Official study title

Osservatorio Regionale Sulla Sindrome metabolicA

Acronym: ORSA Umbria

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Jul 7, 2009
Registry last updated
Oct 13, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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