ID

28606

Descripción

ST Segment Detection Study; ODM derived from: https://clinicaltrials.gov/show/NCT00930969

Link

https://clinicaltrials.gov/show/NCT00930969

Palabras clave

  1. 24/1/18 24/1/18 -
  2. 24/1/18 24/1/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

24 de enero de 2018

DOI

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Licencia

Creative Commons BY-NC 3.0

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Eligibility Coronary Artery Disease NCT00930969

Eligibility Coronary Artery Disease NCT00930969

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
subject is indicated for an icd implantation
Descripción

Indication Implantation of internal cardiac defibrillator

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C1273352
and subject must meet one of the following:
Descripción

Criteria Quantity Fulfill

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C1550543
prior acute coronary event
Descripción

Event Coronary

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0441471
UMLS CUI [1,2]
C1522318
previously underwent percutaneous coronary intervention (pci) or stent procedure
Descripción

Percutaneous Coronary Intervention | Stenting

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C2348535
multivessel disease
Descripción

Disease Vessel multiple

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0005847
UMLS CUI [1,3]
C0439064
positive stress test completed with evidence of ischemic heart disease, as determined by physician, and no subsequent successful revascularization
Descripción

ID.6

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
subject is currently dependent on ventricular pacing
Descripción

Dependence Intraventricular pacing

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0439857
UMLS CUI [1,2]
C0199648
subject has left bundle brunch block (lbbb) and/or wide qrs
Descripción

Left Bundle-Branch Block | Wide QRS complex

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023211
UMLS CUI [2]
C0235475
subject has chronic atrial fibrillation (af)
Descripción

Chronic atrial fibrillation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0694539
subject has dementia
Descripción

Dementia

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0497327
subject is indicated for a single chamber device
Descripción

Indication Single Chamber Pacemaker

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C2911682
subject requires a right sided or abdominal icd implant
Descripción

Patient need for Implantation of internal cardiac defibrillator Right sided | Patient need for Implantation of internal cardiac defibrillator Abdominal

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0686904
UMLS CUI [1,2]
C1273352
UMLS CUI [1,3]
C0444532
UMLS CUI [2,1]
C0686904
UMLS CUI [2,2]
C1273352
UMLS CUI [2,3]
C0000726
subject is pregnant or in fertile age without secure birth control
Descripción

Pregnancy | Childbearing Potential Contraceptive methods Lacking

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2,1]
C3831118
UMLS CUI [2,2]
C0700589
UMLS CUI [2,3]
C0332268
subject has new york heart association (nyha) class iv or refractory heart failure
Descripción

Heart failure New York Heart Association Classification | Refractory heart failure

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
UMLS CUI [2]
C1281998
subject is not expected to survive greater than 12 months
Descripción

Life Expectancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023671
subject is participating in other confounding research studies
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Coronary Artery Disease NCT00930969

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Indication Implantation of internal cardiac defibrillator
Item
subject is indicated for an icd implantation
boolean
C3146298 (UMLS CUI [1,1])
C1273352 (UMLS CUI [1,2])
Criteria Quantity Fulfill
Item
and subject must meet one of the following:
boolean
C0243161 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1550543 (UMLS CUI [1,3])
Event Coronary
Item
prior acute coronary event
boolean
C0441471 (UMLS CUI [1,1])
C1522318 (UMLS CUI [1,2])
Percutaneous Coronary Intervention | Stenting
Item
previously underwent percutaneous coronary intervention (pci) or stent procedure
boolean
C1532338 (UMLS CUI [1,1])
C2348535 (UMLS CUI [1,2])
Disease Vessel multiple
Item
multivessel disease
boolean
C0012634 (UMLS CUI [1,1])
C0005847 (UMLS CUI [1,2])
C0439064 (UMLS CUI [1,3])
ID.6
Item
positive stress test completed with evidence of ischemic heart disease, as determined by physician, and no subsequent successful revascularization
boolean
Item Group
C0680251 (UMLS CUI)
Dependence Intraventricular pacing
Item
subject is currently dependent on ventricular pacing
boolean
C0439857 (UMLS CUI [1,1])
C0199648 (UMLS CUI [1,2])
Left Bundle-Branch Block | Wide QRS complex
Item
subject has left bundle brunch block (lbbb) and/or wide qrs
boolean
C0023211 (UMLS CUI [1])
C0235475 (UMLS CUI [2])
Chronic atrial fibrillation
Item
subject has chronic atrial fibrillation (af)
boolean
C0694539 (UMLS CUI [1])
Dementia
Item
subject has dementia
boolean
C0497327 (UMLS CUI [1])
Indication Single Chamber Pacemaker
Item
subject is indicated for a single chamber device
boolean
C3146298 (UMLS CUI [1,1])
C2911682 (UMLS CUI [1,2])
Patient need for Implantation of internal cardiac defibrillator Right sided | Patient need for Implantation of internal cardiac defibrillator Abdominal
Item
subject requires a right sided or abdominal icd implant
boolean
C0686904 (UMLS CUI [1,1])
C1273352 (UMLS CUI [1,2])
C0444532 (UMLS CUI [1,3])
C0686904 (UMLS CUI [2,1])
C1273352 (UMLS CUI [2,2])
C0000726 (UMLS CUI [2,3])
Pregnancy | Childbearing Potential Contraceptive methods Lacking
Item
subject is pregnant or in fertile age without secure birth control
boolean
C0032961 (UMLS CUI [1])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])
Heart failure New York Heart Association Classification | Refractory heart failure
Item
subject has new york heart association (nyha) class iv or refractory heart failure
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
C1281998 (UMLS CUI [2])
Life Expectancy
Item
subject is not expected to survive greater than 12 months
boolean
C0023671 (UMLS CUI [1])
Study Subject Participation Status
Item
subject is participating in other confounding research studies
boolean
C2348568 (UMLS CUI [1])

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