ID

34217

Descripción

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

Link

https://clinicaltrials.gov/show/NCT01356888

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 NCT01356888

Eligibility Coronary Artery Disease NCT01356888

Criteria
Descripción

Criteria

subject has provided a written informed consent
Descripción

ID.1

Tipo de datos

boolean

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

ID.2

Tipo de datos

boolean

the target lesion length is ≤ 26 mm
Descripción

ID.3

Tipo de datos

boolean

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

ID.4

Tipo de datos

boolean

main exclusion criteria:
Descripción

ID.5

Tipo de datos

boolean

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

ID.6

Tipo de datos

boolean

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

ID.7

Tipo de datos

boolean

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

ID.8

Tipo de datos

boolean

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

ID.9

Tipo de datos

boolean

heavily calcified lesion
Descripción

ID.10

Tipo de datos

boolean

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

ID.11

Tipo de datos

boolean

Similar models

Eligibility Coronary Artery Disease NCT01356888

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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