Awareness of Chinese National Adult Lipid Treatment Guideline (2007) and Rate of Patients Achieving the Treatment Goal
NCT ID: NCT00781560
Last Updated: 2009-08-07
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
2575 participants
OBSERVATIONAL
2008-10-31
2009-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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PROSPECTIVE
Study Groups
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1
patients being diagnosed as dyslipidemia but not receiving Crestor®
No interventions assigned to this group
2
hypercholesterolemia or mixed dyslipidemia and have been initiated treatment with Crestor®
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Having lipids test and record within one months
* Diagnosed as hypercholesterolemia or mixed dyslipidaemias and has been prescribed Crestor® 5mg or 10mg
Exclusion Criteria
18 Years
ALL
No
Sponsors
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AstraZeneca
INDUSTRY
Responsible Party
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AstraZeneca Pharmaceuticals
Principal Investigators
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Karen Atkin
Role: STUDY_DIRECTOR
Astrazeneca China R&D
Zhu Junren
Role: PRINCIPAL_INVESTIGATOR
Fudan University
Locations
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Research Site
Beijing, Beijing Municipality, China
Research Site
Chenzhen, Guangdong, China
Research Site
Guangzhou, Guangdong, China
Research Site
Harbin, Heilongjiang, China
Research Site
Zhengzhou, Henan, China
Research Site
Nanjing, Jiangsu, China
Research Site
Shenyang, Liaoning, China
Research Site
Jinan, Shandong, China
Research Site
Qingdao, Shandong, China
Research Site
Shanghai, Shanghai Municipality, China
Research Site
Xi’an, Shanxi, China
Research Site
Chengdu, Sichuan, China
Research Site
Tianjin, Tianjin Municipality, China
Research Site
Hangzhou, Zhejiang, China
Reseearch Site
Ningbo, Zhejiang, China
Countries
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Other Identifiers
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NIS-CCN-CRE-2008/1
Identifier Type: -
Identifier Source: org_study_id
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