Informações:
Falhas:
ID
22904
Descrição
Drug-eluting Stents to Treat Unprotected Coronary Left Main Disease; ODM derived from: https://clinicaltrials.gov/show/NCT00598637
Link
https://clinicaltrials.gov/show/NCT00598637
Palavras-chave
Versões (1)
- 16/06/2017 16/06/2017 -
Transferido a
16 de junho de 2017
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Coronary Disease NCT00598637
Eligibility Coronary Disease NCT00598637
- StudyEvent: Eligibility
Similar models
Eligibility Coronary Disease NCT00598637
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
ID.1
Item
patients older than age 18 with ischemic symptoms or evidence of myocardial ischemia in the presence of ≥ 50 % stenosis located in unprotected lmca who are unable to undergo cabg because of cardiac surgeons' refusal (poor surgical candidates) or their own unwillingness.
boolean
C0001779 (UMLS CUI [1,1])
C0151744 (UMLS CUI [1,2])
C1261287 (UMLS CUI [1,3])
C0151744 (UMLS CUI [1,2])
C1261287 (UMLS CUI [1,3])
ID.2
Item
pretreatment with a loading dose of 600 mg clopidogrel.
boolean
C0070166 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
ID.3
Item
informed, written consent by the patients or her/his legally-authorized representative for participation in the study.
boolean
C0021430 (UMLS CUI [1])
ID.4
Item
cardiogenic shock.
boolean
C0036980 (UMLS CUI [1])
ID.5
Item
st-segment elevation acute myocardial infarction (st-segment ≥ 0.1 mv elevation in ≥
boolean
C0155626 (UMLS CUI [1,1])
C0520886 (UMLS CUI [1,2])
C0520886 (UMLS CUI [1,2])
ID.6
Item
2 contiguous ecg leads persisting for at least 20 minutes) within 48 hours from symptom onset.
boolean
C0179504 (UMLS CUI [1])
ID.7
Item
in-stent restenosis.
boolean
C3272317 (UMLS CUI [1])
ID.8
Item
malignancies or other comorbid conditions with life expectancy less than one year or that may result in protocol non-compliance.
boolean
C1275743 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,2])
ID.9
Item
prior coronary artery bypass surgery with revascularization of lad and/or lcx.
boolean
C0010055 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
C0262926 (UMLS CUI [1,2])
ID.10
Item
planned staged pci procedure within 30 days from index procedure or prior pci within the last 30 days.
boolean
C1532338 (UMLS CUI [1])
ID.11
Item
an elective surgical procedure is planned that would necessitate interruption of clopidogrel during the first six months post enrollment.
boolean
C0206058 (UMLS CUI [1])
ID.12
Item
known allergy to the study medications: aspirin, clopidogrel, uhf; sirolimus, paclitaxel; true anaphylaxis after prior exposure to contrast media.
boolean
C0020517 (UMLS CUI [1])
ID.13
Item
pregnancy (present, suspected or planned).
boolean
C0032961 (UMLS CUI [1,1])
C0425965 (UMLS CUI [1,2])
C0425965 (UMLS CUI [1,2])
ID.14
Item
patient's inability to fully cooperate with the study protocol.
boolean
C1321605 (UMLS CUI [1])