Centralized Pan-Middle East Survey on the Undertreatment of Hypercholesterolemia
NCT ID: NCT01025388
Last Updated: 2013-02-08
Study Results
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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COMPLETED
4053 participants
OBSERVATIONAL
2009-11-30
2010-05-31
Brief Summary
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* Primary/secondary prevention patients.
* Patients with metabolic syndrome (according to NCEP III definition).
In addition, the purpose is to establish the proportion of patients on lipid-lowering pharmacological treatment reaching the LDL-C goals according to the Third Joint European Task Force guidelines/national guidelines, in the survey population and in the following sub-populations:
* Primary/secondary prevention patients.
* Patients with metabolic syndrome.
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
* Subject must sign informed consent
Exclusion Criteria
18 Years
ALL
No
Sponsors
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ClinArt Company & Signen Clinical Discoveries
UNKNOWN
AstraZeneca
INDUSTRY
Responsible Party
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Principal Investigators
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Prof. Mohammed Arafah
Role: STUDY_CHAIR
King Khalid University Hospital
Dr. Shorook Alherz
Role: PRINCIPAL_INVESTIGATOR
King Fahad National Guard Hospital
Dr. Khalid Alnemer
Role: PRINCIPAL_INVESTIGATOR
Security Forces Hospital
Dr. Hossam Alghetany
Role: PRINCIPAL_INVESTIGATOR
Soliman Fakieh Hospital
Dr. Othman Metwally
Role: PRINCIPAL_INVESTIGATOR
King Fahad General Hospital
Dr. Akram Alkhadra
Role: PRINCIPAL_INVESTIGATOR
King Fahad University Hospital
Dr. Faisal Alanizi
Role: PRINCIPAL_INVESTIGATOR
Ministry of Health, Saudi Arabia
Locations
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Research Site
Riyadh, Central, Saudi Arabia
Research Site
Dammam, Eastern Province, Saudi Arabia
Research Site
Aljouf, North, Saudi Arabia
Research Site
Jeddah, Western, Saudi Arabia
Research Site
Makah, Western, Saudi Arabia
Countries
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Other Identifiers
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NIS-SA-CRE-2009/1
Identifier Type: -
Identifier Source: org_study_id
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