ID

34217

Description

Study of the Orsiro Drug Eluting Stent System; ODM derived from: https://clinicaltrials.gov/show/NCT01356888

Link

https://clinicaltrials.gov/show/NCT01356888

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 NCT01356888

Eligibility Coronary Artery Disease NCT01356888

Criteria
Description

Criteria

subject has provided a written informed consent
Description

ID.1

Data type

boolean

single de novo lesion with ≥ 50% and <100% stenosis in up to 2 coronary arteries
Description

ID.2

Data type

boolean

the target lesion length is ≤ 26 mm
Description

ID.3

Data type

boolean

the target reference vessel diameter is ≥ 2.25 mm and ≤ 4.0 mm
Description

ID.4

Data type

boolean

main exclusion criteria:
Description

ID.5

Data type

boolean

evidence of myocardial infarction within 72 hours prior to index procedure
Description

ID.6

Data type

boolean

unprotected left main coronary artery disease (stenosis >50%)
Description

ID.7

Data type

boolean

three-vessel coronary artery disease at time of procedure thrombus in target vessel
Description

ID.8

Data type

boolean

target lesion involves a side branch > 2.0 mm in diameter
Description

ID.9

Data type

boolean

heavily calcified lesion
Description

ID.10

Data type

boolean

target lesion is located in or supplied by an arterial or venous bypass graft
Description

ID.11

Data type

boolean

Similar models

Eligibility Coronary Artery Disease NCT01356888

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
ID.1
Item
subject has provided a written informed consent
boolean
ID.2
Item
single de novo lesion with ≥ 50% and <100% stenosis in up to 2 coronary arteries
boolean
ID.3
Item
the target lesion length is ≤ 26 mm
boolean
ID.4
Item
the target reference vessel diameter is ≥ 2.25 mm and ≤ 4.0 mm
boolean
ID.5
Item
main exclusion criteria:
boolean
ID.6
Item
evidence of myocardial infarction within 72 hours prior to index procedure
boolean
ID.7
Item
unprotected left main coronary artery disease (stenosis >50%)
boolean
ID.8
Item
three-vessel coronary artery disease at time of procedure thrombus in target vessel
boolean
ID.9
Item
target lesion involves a side branch > 2.0 mm in diameter
boolean
ID.10
Item
heavily calcified lesion
boolean
ID.11
Item
target lesion is located in or supplied by an arterial or venous bypass graft
boolean

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