ID

28467

Description

Protect II, A Prospective, Multicenter Randomized Controlled Trial; ODM derived from: https://clinicaltrials.gov/show/NCT00562016

Link

https://clinicaltrials.gov/show/NCT00562016

Keywords

  1. 1/16/18 1/16/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

January 16, 2018

DOI

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License

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT00562016

Eligibility Coronary Artery Disease NCT00562016

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
subject is indicated for a non emergent percutaneous treatment of at least on de novo or restenotic lesion in a native coronary vessel or bypass graft.
Description

Indication Therapeutic procedure Percutaneous | Lesion de novo Quantity Coronary Vessel | Restenotic lesion of coronary artery Quantity | Lesion de novo Quantity Bypass graft

Data type

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C0522523
UMLS CUI [2,1]
C0221198
UMLS CUI [2,2]
C1515568
UMLS CUI [2,3]
C1265611
UMLS CUI [2,4]
C0010075
UMLS CUI [3,1]
C1299362
UMLS CUI [3,2]
C1265611
UMLS CUI [4,1]
C0221198
UMLS CUI [4,2]
C1515568
UMLS CUI [4,3]
C1265611
UMLS CUI [4,4]
C0185098
patient presents with:
Description

Presentation

Data type

boolean

Alias
UMLS CUI [1]
C0449450
a compromised ejection fraction
Description

Ejection fraction Impaired

Data type

boolean

Alias
UMLS CUI [1,1]
C2700378
UMLS CUI [1,2]
C0221099
intervention on the last patent coronary conduit
Description

Intervention Other Coding

Data type

boolean

Alias
UMLS CUI [1,1]
C0184661
UMLS CUI [1,2]
C3846158
intervention on an unprotected left main artery or
Description

Intervention Left main coronary artery

Data type

boolean

Alias
UMLS CUI [1,1]
C0184661
UMLS CUI [1,2]
C1261082
patient presenting with triple vessel disease.
Description

Triple vessel disease

Data type

boolean

Alias
UMLS CUI [1]
C0856738
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
st elevation m.i.
Description

ST segment elevation myocardial infarction

Data type

boolean

Alias
UMLS CUI [1]
C1536220
pre procedure cardiac arrest within 24 hours.
Description

Cardiac Arrest Pre-Procedure

Data type

boolean

Alias
UMLS CUI [1,1]
C0018790
UMLS CUI [1,2]
C3272300
subject in cardiogenic shock
Description

Shock, Cardiogenic

Data type

boolean

Alias
UMLS CUI [1]
C0036980

Similar models

Eligibility Coronary Artery Disease NCT00562016

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
Indication Therapeutic procedure Percutaneous | Lesion de novo Quantity Coronary Vessel | Restenotic lesion of coronary artery Quantity | Lesion de novo Quantity Bypass graft
Item
subject is indicated for a non emergent percutaneous treatment of at least on de novo or restenotic lesion in a native coronary vessel or bypass graft.
boolean
C3146298 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0522523 (UMLS CUI [1,3])
C0221198 (UMLS CUI [2,1])
C1515568 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C0010075 (UMLS CUI [2,4])
C1299362 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C0221198 (UMLS CUI [4,1])
C1515568 (UMLS CUI [4,2])
C1265611 (UMLS CUI [4,3])
C0185098 (UMLS CUI [4,4])
Presentation
Item
patient presents with:
boolean
C0449450 (UMLS CUI [1])
Ejection fraction Impaired
Item
a compromised ejection fraction
boolean
C2700378 (UMLS CUI [1,1])
C0221099 (UMLS CUI [1,2])
Intervention Other Coding
Item
intervention on the last patent coronary conduit
boolean
C0184661 (UMLS CUI [1,1])
C3846158 (UMLS CUI [1,2])
Intervention Left main coronary artery
Item
intervention on an unprotected left main artery or
boolean
C0184661 (UMLS CUI [1,1])
C1261082 (UMLS CUI [1,2])
Triple vessel disease
Item
patient presenting with triple vessel disease.
boolean
C0856738 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ST segment elevation myocardial infarction
Item
st elevation m.i.
boolean
C1536220 (UMLS CUI [1])
Cardiac Arrest Pre-Procedure
Item
pre procedure cardiac arrest within 24 hours.
boolean
C0018790 (UMLS CUI [1,1])
C3272300 (UMLS CUI [1,2])
Shock, Cardiogenic
Item
subject in cardiogenic shock
boolean
C0036980 (UMLS CUI [1])

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