ID

11707

Beschrijving

This present study is specifically designed to examine the efficacy and safety of a high pre-treatment dose of atorvastatin in Asian patients with NSTE-ACS in China and the Republic of Korea, by using a treatment paradigm similar to that employed in the ARMYDA-ACS study. https://clinicaltrials.gov/ct2/show/NCT00728988

Link

https://clinicaltrials.gov/ct2/show/NCT00728988

Trefwoorden

  1. 28-07-15 28-07-15 -
Geüploaded op

28 juli 2015

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility ALPACS Acute Coronary Syndrome NCT00728988

Eligibility Criteria

  1. StudyEvent: ODM
    1. Eligibility Criteria
Inclusion Criteria
Beschrijving

Inclusion Criteria

Non-ST elevated ACS
Beschrijving

Non-ST elevated ACS

Datatype

boolean

Alias
UMLS CUI-1
C3537184
LDL-C > 80 mg/dl
Beschrijving

LDL-C > 80 mg/dl

Datatype

boolean

Alias
UMLS CUI-1
C0428474
Exclusion Criteria
Beschrijving

Exclusion Criteria

ST elevated acute myocardial infarction
Beschrijving

ST elevated acute myocardial infarction

Datatype

boolean

Alias
UMLS CUI-1
C1536220
Previously or currently treated with atorvastatin or other statins
Beschrijving

Previously or currently treated with atorvastatin or other statins

Datatype

boolean

Alias
UMLS CUI-1
C0360714

Similar models

Eligibility Criteria

  1. StudyEvent: ODM
    1. Eligibility Criteria
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Inclusion Criteria
NSTEMI
Item
Non-ST elevated ACS
boolean
C3537184 (UMLS CUI-1)
LDL
Item
LDL-C > 80 mg/dl
boolean
C0428474 (UMLS CUI-1)
Item Group
Exclusion Criteria
STEMI
Item
ST elevated acute myocardial infarction
boolean
C1536220 (UMLS CUI-1)
Statins
Item
Previously or currently treated with atorvastatin or other statins
boolean
C0360714 (UMLS CUI-1)

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