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Centralized Pan-Asian Survey on the Under Treatment of Hypercholesterolemia

Completed
Conditions
Hypercholesterolemia
Registration Number
NCT00687492
Lead Sponsor
AstraZeneca
Brief Summary

The survey will try to establish the proportion of patients on lipid-lowering pharmacological treatment reaching the LDL-C goals according to the third NCEP ATP guidelines, overall and by country.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
8000
Inclusion Criteria
  • 2 or more risk factors (according to NCEP ATP III guideline)
  • Receiving lipid-lowering drug treatment for at least 3 months without dosage change for a minimum of 6 weeks.
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Exclusion Criteria
  • Involvement in the planning and conduct of the study (applies to both AstraZeneca staff or staff at the study site).
  • Previous enrolment or randomisation of treatment in the present study.
  • Participation in a clinical study during the last 90 days.
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The number and percentage of subjects achieving the LDL-C goals according to updated 2004 NCEP ATP Ⅲ guidelines(overall and by country)After collecting all Patient Record Form.
Secondary Outcome Measures
NameTimeMethod
The number and percentage of subjects achieving the LDL-C goals according to the updated 2004 NCEP ATP Ⅲ guidelines for several subject subsets.After collecting all Patient Record Form.
The association between achievement of LDL-C goals,according to the updated 2004 NCEP ATPⅢ guidelines and patient and physician variables.After collecting all Patient Record Form.
The physician characteristics associated with the allocation of hypercholesterolemia treatment regime.After collecting all Patient Record Form.

Trial Locations

Locations (1)

Research Site

🇻🇳

Hcmc, Vietnam

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