ID

11707

Descripción

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

Palabras clave

  1. 28/7/15 28/7/15 -
Subido en

28 de julio de 2015

DOI

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Licencia

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
Descripción

Inclusion Criteria

Non-ST elevated ACS
Descripción

Non-ST elevated ACS

Tipo de datos

boolean

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

LDL-C > 80 mg/dl

Tipo de datos

boolean

Alias
UMLS CUI-1
C0428474
Exclusion Criteria
Descripción

Exclusion Criteria

ST elevated acute myocardial infarction
Descripción

ST elevated acute myocardial infarction

Tipo de datos

boolean

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

Previously or currently treated with atorvastatin or other statins

Tipo de datos

boolean

Alias
UMLS CUI-1
C0360714

Similar models

Eligibility Criteria

  1. StudyEvent: ODM
    1. Eligibility Criteria
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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