ID

34231

Description

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

Keywords

  1. 1/15/19 1/15/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 15, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT02155530

Eligibility Coronary Artery Disease NCT02155530

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient is ≥ 20 years old
Description

ID.1

Data type

boolean

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

ID.2

Data type

boolean

patients who received des within 1 year before oct evaluation
Description

ID.3

Data type

boolean

patients with homogenous or hetero neointimal pattern by oct
Description

ID.4

Data type

boolean

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

ID.5

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
refuse to participate
Description

ID.6

Data type

boolean

contraindication to statin treatment
Description

ID.7

Data type

boolean

women with current or potential childbearing
Description

ID.8

Data type

boolean

life expectancy <1 year
Description

ID.9

Data type

boolean

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

ID.10

Data type

boolean

Similar models

Eligibility Coronary Artery Disease NCT02155530

Name
Type
Description | Question | Decode (Coded Value)
Data type
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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