Informatie:
Fout:
ID
13620
Beschrijving
The Stent or Surgery (SoS) Trial; ODM derived from: https://clinicaltrials.gov/show/NCT00475449
Link
https://clinicaltrials.gov/show/NCT00475449
Trefwoorden
Versies (1)
- 20-02-16 20-02-16 -
Geüploaded op
20 februari 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT00475449
Eligibility Coronary Artery Disease NCT00475449
- StudyEvent: Eligibility
Similar models
Eligibility Coronary Artery Disease NCT00475449
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
written informed consent
Item
written informed consent.
boolean
C0021430 (UMLS CUI [1])
angina pectoris
Item
patient has typical angina pectoris - stable or unstable symptoms.
boolean
C0002962 (UMLS CUI [1])
atherosclerotic coronary artery disease
Item
atherosclerotic coronary artery disease demonstrated with selective coronary angiography with a significant lesion present in at least two of the principal epicardial vessel systems.
boolean
C0010054 (UMLS CUI [1])
revascularisation indicated
Item
revascularisation procedure clinically indicated.
boolean
C0581603 (UMLS CUI [1,1])
C1444656 (UMLS CUI [1,2])
C1444656 (UMLS CUI [1,2])
cabg
Item
nominated trial surgeon accepts the patient for cabg.
boolean
C0010055 (UMLS CUI [1,1])
C1444656 (UMLS CUI [1,2])
C1444656 (UMLS CUI [1,2])
ptca and stent indicated
Item
nominated trial interventionist accepts the patient for ptca and stent.
boolean
C2936173 (UMLS CUI [1,1])
C1444656 (UMLS CUI [1,2])
C1444656 (UMLS CUI [1,2])
stent indicated
Item
at least one identified lesion suitable and targeted for primary stent implantation.
boolean
C0038257 (UMLS CUI [1,1])
C1444656 (UMLS CUI [1,2])
C1444656 (UMLS CUI [1,2])
revascularisation strategy can be performed within 6 weeks of randomisation
Item
a procedure for the completion of either revascularisation strategy can be performed within 6 weeks of randomisation.
boolean
C1321605 (UMLS CUI [1])
previous cabg procedure or other thoracotomy
Item
previous cabg procedure or other thoracotomy.
boolean
C0010055 (UMLS CUI [1])
C0039991 (UMLS CUI [2])
C0039991 (UMLS CUI [2])
previous coronary intervention
Item
previous coronary interventional procedure (of any type).
boolean
C1532338 (UMLS CUI [1])
intervention on cardiac valve scheduled for revascularisation procedure
Item
intervention on any cardiac valve scheduled for the index revascularisation procedure.
boolean
C3274795 (UMLS CUI [1])
intervention on the myocardium scheduled for the revascularisation procedure
Item
excision or other intervention on the myocardium scheduled for the index revascularisation procedure.
boolean
C0027061 (UMLS CUI [1])
intervention on the great vessels scheduled for the revascularisation procedure
Item
intervention on the great vessels, carotid arteries or aorta scheduled for the index revascularisation procedure.
boolean
C1292969 (UMLS CUI [1])
absent autograft material
Item
absent autologous graft material.
boolean
C0559189 (UMLS CUI [1])
disease influencing survival
Item
non-cardiac disease influencing survival.
boolean
C0009488 (UMLS CUI [1])
acute myocardial infarction
Item
acute myocardial infarction in the 48 hours preceding the proposed revascularisation procedure.
boolean
C0155626 (UMLS CUI [1])
participation in any other study
Item
participation in any other study that would involve deviation from the routine local management of a revascularisation procedure.
boolean
C2348568 (UMLS CUI [1])
allergy to locally used anti-platelet agents
Item
allergy to anti-platelet agents in local use.
boolean
C0020517 (UMLS CUI [1,1])
C2963157 (UMLS CUI [1,2])
C2963157 (UMLS CUI [1,2])
communication barriers
Item
language or other communication barrier.
boolean
C1321605 (UMLS CUI [1])
follow up limited
Item
follow-up for two years not possible / patient unreliable.
boolean
C1321605 (UMLS CUI [1])