Study identifier:NIS-CCN-CRE-2008/1
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A cross-sectional study to survey the awareness of Chinese National Adult Lipid Treatment Guideline (2007) and the rate of patients (on treatment) achieving the hyperlipidaemia treatment goal with Crestor 5mg to 10mg for 8 weeks
hyperlipidemia
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No
-
All
2575
Observational
18 Years +
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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No locations available
Arms | Assigned Interventions |
---|---|
1 patients being diagnosed as dyslipidemia but not receiving Crestor® | - |
2 hypercholesterolemia or mixed dyslipidemia and have been initiated treatment with Crestor® | - |