ID

34232

Description

POLish Bifurcation Optimal Stenting Study; ODM derived from: https://clinicaltrials.gov/show/NCT02192840

Link

https://clinicaltrials.gov/show/NCT02192840

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 NCT02192840

Eligibility Coronary Artery Disease NCT02192840

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
subject able to verbally confirm understandings of risks, benefits of receiving pci for true bifurcation lesions, and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure.
Description

ID.1

Data type

boolean

target main branch lesion(s) located in a native coronary artery with diameter of ≥
Description

ID.2

Data type

boolean

2.5 mm and ≤ 4.5 mm. target side branch lesion(s) located in a native coronary artery with diameter of ≥ 2.0 mm.
Description

ID.3

Data type

boolean

target lesion(s) amenable for pci with balloon angioplasty of the side branch.
Description

ID.4

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
stemi
Description

ID.5

Data type

boolean

non-cardiac co-morbid conditions are present with life expectancy <1 year or that may result in protocol non-compliance (per site investigator's medical judgment).
Description

ID.6

Data type

boolean

subjects who refuse to give informed consent.
Description

ID.7

Data type

boolean

subjects with lvef<30%
Description

ID.8

Data type

boolean

subjects with moderate or severe degree valvular heart disease or primary cardiomyopathy
Description

ID.9

Data type

boolean

Similar models

Eligibility Coronary Artery Disease NCT02192840

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
subject able to verbally confirm understandings of risks, benefits of receiving pci for true bifurcation lesions, and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure.
boolean
ID.2
Item
target main branch lesion(s) located in a native coronary artery with diameter of ≥
boolean
ID.3
Item
2.5 mm and ≤ 4.5 mm. target side branch lesion(s) located in a native coronary artery with diameter of ≥ 2.0 mm.
boolean
ID.4
Item
target lesion(s) amenable for pci with balloon angioplasty of the side branch.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
stemi
boolean
ID.6
Item
non-cardiac co-morbid conditions are present with life expectancy <1 year or that may result in protocol non-compliance (per site investigator's medical judgment).
boolean
ID.7
Item
subjects who refuse to give informed consent.
boolean
ID.8
Item
subjects with lvef<30%
boolean
ID.9
Item
subjects with moderate or severe degree valvular heart disease or primary cardiomyopathy
boolean

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