ID

41550

Beskrivning

Complete Infarct Related Artery Revascularization; ODM derived from: https://clinicaltrials.gov/show/NCT01218815

Länk

https://clinicaltrials.gov/show/NCT01218815

Nyckelord

Versioner (1)
  1. 2020-11-05 2020-11-05 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

5 november 2020

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0
Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Tillbaka till modellkommentarer
Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility Myocardial Infarction NCT01218815

Engelsk

Eligibility Myocardial Infarction NCT01218815

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of stemi (according to esc 2007 definition)
Beskrivning

diagnosis of stemi

Datatyp

boolean

Alias
UMLS CUI [1]
C1536220
chest pain onset <12 hours
Beskrivning

chest pain onset

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0008031
UMLS CUI [1,2]
C0449244
signed informed consent
Beskrivning

signed informed consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
presence of two critical lesions requiring pci in ira (lad - left anterior descending, cx - circumflex, rca - right coronary artery)
Beskrivning

presence of two critical lesions requiring pci in LAD, CX or RCA

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1511545
UMLS CUI [1,2]
C0221198
UMLS CUI [1,3]
C1514873
UMLS CUI [1,4]
C1532338
UMLS CUI [1,5]
C0226032
UMLS CUI [2,1]
C1511545
UMLS CUI [2,2]
C0221198
UMLS CUI [2,3]
C1514873
UMLS CUI [2,4]
C1532338
UMLS CUI [2,5]
C0226037
UMLS CUI [3,1]
C1511545
UMLS CUI [3,2]
C0221198
UMLS CUI [3,3]
C1514873
UMLS CUI [3,4]
C1532338
UMLS CUI [3,5]
C0226042
target/culprit lesion which requires immediate stenting (>50 - 100%) and second critical lesion (70-90%) with timi 3 flow after pci of the 1st target/culprit lesion
Beskrivning

target/culprit lesion requiring immediate stenting and second critical lesion with timi 3 flow after PCI of the first target/culprit lesion

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1299364
UMLS CUI [1,2]
C2348535
UMLS CUI [1,3]
C0205253
UMLS CUI [2,1]
C1299364
UMLS CUI [2,2]
C0205436
UMLS CUI [2,3]
C3272266
UMLS CUI [2,4]
C0687676
UMLS CUI [2,5]
C1532338
over 18 years of age
Beskrivning

age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
ira diameter ≥ 2.5 mm
Beskrivning

infarct related artery diameter

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0003842
UMLS CUI [1,2]
C0027051
UMLS CUI [1,3]
C1301886
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
terminal illness with life expectancy less <1 year or active cancer disease
Beskrivning

terminal illness with low life expectancy or active cancer disease

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0679247
UMLS CUI [1,2]
C0023671
UMLS CUI [2,1]
C0006826
UMLS CUI [2,2]
C0205177
pregnancy or possibility of pregnancy
Beskrivning

pregnancy or possibility of pregnancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0425965
second critical lesion in ira >90% or occlusion
Beskrivning

second critical lesion in ira or occlusion

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1511545
UMLS CUI [1,3]
C0205436
UMLS CUI [1,4]
C0003842
UMLS CUI [1,5]
C0027051
UMLS CUI [2,1]
C0205436
UMLS CUI [2,2]
C0221198
UMLS CUI [2,3]
C0151814
contraindications to pci or/and stent implantation
Beskrivning

contraindications to pci or/and stent implantation

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C1532338
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0521232
contraindications to des stent implantation
Beskrivning

contraindications to des stent implantation

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C1322815
lesion diameters unsuitable for intended stent platform
Beskrivning

lesion diameters unsuitable for intended stent platform

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1301886
UMLS CUI [1,3]
C1548788
UMLS CUI [1,4]
C0038257
active bleeding or coagulopathy
Beskrivning

active bleeding or coagulopathy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0205177
UMLS CUI [1,2]
C0019080
UMLS CUI [2,1]
C0205177
UMLS CUI [2,2]
C0005779
patient in cardiogenic shock (<90mmhg sbp and/or requiring iabp - intraaortic balloon pump - or vasopressors) - killip 4 class
Beskrivning

patient in cardiogenic shock - killip 4 class

Datatyp

boolean

Alias
UMLS CUI [1]
C0036980
UMLS CUI [2]
C1881332
patient has left bundle branch block (lbbb) or pacemaker rhythm
Beskrivning

left bundle branch block (lbbb) or pacemaker rhythm

Datatyp

boolean

Alias
UMLS CUI [1]
C0023211
UMLS CUI [2]
C1167946
no future patient cooperation expected
Beskrivning

no future patient cooperation expected

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0016884
UMLS CUI [1,2]
C0392337
UMLS CUI [1,3]
C3841878
patient is participating in another clinical study
Beskrivning

participating in another clinical study

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C3274035
Tillbaka till toppen

Similar models

Eligibility Myocardial Infarction NCT01218815

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
diagnosis of stemi
Item
diagnosis of stemi (according to esc 2007 definition)
boolean
C1536220 (UMLS CUI [1])
chest pain onset
Item
chest pain onset <12 hours
boolean
C0008031 (UMLS CUI [1,1])
C0449244 (UMLS CUI [1,2])
signed informed consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
presence of two critical lesions requiring pci in LAD, CX or RCA
Item
presence of two critical lesions requiring pci in ira (lad - left anterior descending, cx - circumflex, rca - right coronary artery)
boolean
C1511545 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C1514873 (UMLS CUI [1,3])
C1532338 (UMLS CUI [1,4])
C0226032 (UMLS CUI [1,5])
C1511545 (UMLS CUI [2,1])
C0221198 (UMLS CUI [2,2])
C1514873 (UMLS CUI [2,3])
C1532338 (UMLS CUI [2,4])
C0226037 (UMLS CUI [2,5])
C1511545 (UMLS CUI [3,1])
C0221198 (UMLS CUI [3,2])
C1514873 (UMLS CUI [3,3])
C1532338 (UMLS CUI [3,4])
C0226042 (UMLS CUI [3,5])
target/culprit lesion requiring immediate stenting and second critical lesion with timi 3 flow after PCI of the first target/culprit lesion
Item
target/culprit lesion which requires immediate stenting (>50 - 100%) and second critical lesion (70-90%) with timi 3 flow after pci of the 1st target/culprit lesion
boolean
C1299364 (UMLS CUI [1,1])
C2348535 (UMLS CUI [1,2])
C0205253 (UMLS CUI [1,3])
C1299364 (UMLS CUI [2,1])
C0205436 (UMLS CUI [2,2])
C3272266 (UMLS CUI [2,3])
C0687676 (UMLS CUI [2,4])
C1532338 (UMLS CUI [2,5])
age
Item
over 18 years of age
boolean
C0001779 (UMLS CUI [1])
infarct related artery diameter
Item
ira diameter ≥ 2.5 mm
boolean
C0003842 (UMLS CUI [1,1])
C0027051 (UMLS CUI [1,2])
C1301886 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
terminal illness with low life expectancy or active cancer disease
Item
terminal illness with life expectancy less <1 year or active cancer disease
boolean
C0679247 (UMLS CUI [1,1])
C0023671 (UMLS CUI [1,2])
C0006826 (UMLS CUI [2,1])
C0205177 (UMLS CUI [2,2])
pregnancy or possibility of pregnancy
Item
pregnancy or possibility of pregnancy
boolean
C0032961 (UMLS CUI [1])
C0425965 (UMLS CUI [2])
second critical lesion in ira or occlusion
Item
second critical lesion in ira >90% or occlusion
boolean
C0221198 (UMLS CUI [1,1])
C1511545 (UMLS CUI [1,2])
C0205436 (UMLS CUI [1,3])
C0003842 (UMLS CUI [1,4])
C0027051 (UMLS CUI [1,5])
C0205436 (UMLS CUI [2,1])
C0221198 (UMLS CUI [2,2])
C0151814 (UMLS CUI [2,3])
contraindications to pci or/and stent implantation
Item
contraindications to pci or/and stent implantation
boolean
C1301624 (UMLS CUI [1,1])
C1532338 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0521232 (UMLS CUI [2,2])
contraindications to des stent implantation
Item
contraindications to des stent implantation
boolean
C1301624 (UMLS CUI [1,1])
C1322815 (UMLS CUI [1,2])
lesion diameters unsuitable for intended stent platform
Item
lesion diameters unsuitable for intended stent platform
boolean
C0221198 (UMLS CUI [1,1])
C1301886 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])
C0038257 (UMLS CUI [1,4])
active bleeding or coagulopathy
Item
active bleeding or coagulopathy
boolean
C0205177 (UMLS CUI [1,1])
C0019080 (UMLS CUI [1,2])
C0205177 (UMLS CUI [2,1])
C0005779 (UMLS CUI [2,2])
patient in cardiogenic shock - killip 4 class
Item
patient in cardiogenic shock (<90mmhg sbp and/or requiring iabp - intraaortic balloon pump - or vasopressors) - killip 4 class
boolean
C0036980 (UMLS CUI [1])
C1881332 (UMLS CUI [2])
left bundle branch block (lbbb) or pacemaker rhythm
Item
patient has left bundle branch block (lbbb) or pacemaker rhythm
boolean
C0023211 (UMLS CUI [1])
C1167946 (UMLS CUI [2])
no future patient cooperation expected
Item
no future patient cooperation expected
boolean
C0016884 (UMLS CUI [1,1])
C0392337 (UMLS CUI [1,2])
C3841878 (UMLS CUI [1,3])
participating in another clinical study
Item
patient is participating in another clinical study
boolean
C2348568 (UMLS CUI [1,1])
C3274035 (UMLS CUI [1,2])
Tillbaka till toppen 

Kontakt

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Hjälp

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial