ID

34231

Descripción

COmparison and Modification in Neointimal Pattern Assessed by Optical Coherence Tomography With High Versus Moderate Efficacy Statin Treatment After Drug Eluting Stent Implantation: COMPASS Trial; ODM derived from: https://clinicaltrials.gov/show/NCT02155530

Link

https://clinicaltrials.gov/show/NCT02155530

Palabras clave

  1. 15/1/19 15/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

15 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT02155530

Eligibility Coronary Artery Disease NCT02155530

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient is ≥ 20 years old
Descripción

ID.1

Tipo de datos

boolean

patients who received oct related to clinical needs or the end point of other study
Descripción

ID.2

Tipo de datos

boolean

patients who received des within 1 year before oct evaluation
Descripción

ID.3

Tipo de datos

boolean

patients with homogenous or hetero neointimal pattern by oct
Descripción

ID.4

Tipo de datos

boolean

non-statin user and moderate or low efficacy statin user
Descripción

ID.5

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
refuse to participate
Descripción

ID.6

Tipo de datos

boolean

contraindication to statin treatment
Descripción

ID.7

Tipo de datos

boolean

women with current or potential childbearing
Descripción

ID.8

Tipo de datos

boolean

life expectancy <1 year
Descripción

ID.9

Tipo de datos

boolean

high efficacy statin user (atorvastatin 80mg or rosuvastatin 20mg)
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Coronary Artery Disease NCT02155530

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patient is ≥ 20 years old
boolean
ID.2
Item
patients who received oct related to clinical needs or the end point of other study
boolean
ID.3
Item
patients who received des within 1 year before oct evaluation
boolean
ID.4
Item
patients with homogenous or hetero neointimal pattern by oct
boolean
ID.5
Item
non-statin user and moderate or low efficacy statin user
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
refuse to participate
boolean
ID.7
Item
contraindication to statin treatment
boolean
ID.8
Item
women with current or potential childbearing
boolean
ID.9
Item
life expectancy <1 year
boolean
ID.10
Item
high efficacy statin user (atorvastatin 80mg or rosuvastatin 20mg)
boolean

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