Study On Liprimar (Atorvastatin) In Patients With Coronary Heart Disease (CHD) And High Risk Of Cardiovascular Complications
NCT ID: NCT00993915
Last Updated: 2021-02-18
Study Results
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View full resultsBasic Information
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COMPLETED
687 participants
OBSERVATIONAL
2010-04-30
2011-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Main group
Newly diagnosed or known coronary artery disease and known dislipidemia and high risk of cardiovascular complications
Atorvastatin
Atorvastatin, 10- 80 mg, once daily, 6 month treatment
Interventions
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Atorvastatin
Atorvastatin, 10- 80 mg, once daily, 6 month treatment
Eligibility Criteria
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Inclusion Criteria
* Patients with indications to lipid lowing therapy, according to local product document.
* Patients with CHD and high risk of CV complications (Diabetes Mellitus II, Myocardial Infarction, Heart Failure, Arterial Hypertension, ets) will be included into study;
* Patients with LDL levels: \> 3,5 mmol/l
Exclusion Criteria
18 Years
80 Years
ALL
No
Sponsors
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Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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Pfizer CT.gov Call Center
Role: STUDY_DIRECTOR
Pfizer
Related Links
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To obtain contact information for a study center near you, click here.
Other Identifiers
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A2581185
Identifier Type: -
Identifier Source: org_study_id
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