ID

34220

Beschrijving

BIOFLOW-INDIA Safety and Clinical PerFormance of the Drug Eluting ORSIRO Stent in Single de Novo Coronary Artery Lesions; ODM derived from: https://clinicaltrials.gov/show/NCT01426139

Link

https://clinicaltrials.gov/show/NCT01426139

Trefwoorden

  1. 15-01-19 15-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

15 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT01426139

Eligibility Coronary Artery Disease NCT01426139

Criteria
Beschrijving

Criteria

subject has provided a written informed consent
Beschrijving

ID.1

Datatype

boolean

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

ID.2

Datatype

boolean

the target lesion length is ≤ 26 mm
Beschrijving

ID.3

Datatype

boolean

the target reference vessel diameter is ≥ 2.0 mm and ≤ 4.0 mm
Beschrijving

ID.4

Datatype

boolean

main exclusion criteria:
Beschrijving

ID.5

Datatype

boolean

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

ID.6

Datatype

boolean

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

ID.7

Datatype

boolean

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

ID.8

Datatype

boolean

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

ID.9

Datatype

boolean

heavily calcified lesion
Beschrijving

ID.10

Datatype

boolean

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

ID.11

Datatype

boolean

Similar models

Eligibility Coronary Artery Disease NCT01426139

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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 ≥ 2.0 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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