ID

22904

Description

Drug-eluting Stents to Treat Unprotected Coronary Left Main Disease; ODM derived from: https://clinicaltrials.gov/show/NCT00598637

Link

https://clinicaltrials.gov/show/NCT00598637

Keywords

Versions (1)
  1. 6/16/17 6/16/17 -
Uploaded on

June 16, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Coronary Disease NCT00598637

English

Eligibility Coronary Disease NCT00598637

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
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.
Description

ID.1

Data type

boolean

Alias
UMLS CUI [1,1]
C0001779
UMLS CUI [1,2]
C0151744
UMLS CUI [1,3]
C1261287
pretreatment with a loading dose of 600 mg clopidogrel.
Description

ID.2

Data type

boolean

Alias
UMLS CUI [1,1]
C0070166
UMLS CUI [1,2]
C0178602
informed, written consent by the patients or her/his legally-authorized representative for participation in the study.
Description

ID.3

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
cardiogenic shock.
Description

ID.4

Data type

boolean

Alias
UMLS CUI [1]
C0036980
st-segment elevation acute myocardial infarction (st-segment ≥ 0.1 mv elevation in ≥
Description

ID.5

Data type

boolean

Alias
UMLS CUI [1,1]
C0155626
UMLS CUI [1,2]
C0520886
2 contiguous ecg leads persisting for at least 20 minutes) within 48 hours from symptom onset.
Description

ID.6

Data type

boolean

Alias
UMLS CUI [1]
C0179504
in-stent restenosis.
Description

ID.7

Data type

boolean

Alias
UMLS CUI [1]
C3272317
malignancies or other comorbid conditions with life expectancy less than one year or that may result in protocol non-compliance.
Description

ID.8

Data type

boolean

Alias
UMLS CUI [1,1]
C1275743
UMLS CUI [1,2]
C0006826
prior coronary artery bypass surgery with revascularization of lad and/or lcx.
Description

ID.9

Data type

boolean

Alias
UMLS CUI [1,1]
C0010055
UMLS CUI [1,2]
C0262926
planned staged pci procedure within 30 days from index procedure or prior pci within the last 30 days.
Description

ID.10

Data type

boolean

Alias
UMLS CUI [1]
C1532338
an elective surgical procedure is planned that would necessitate interruption of clopidogrel during the first six months post enrollment.
Description

ID.11

Data type

boolean

Alias
UMLS CUI [1]
C0206058
known allergy to the study medications: aspirin, clopidogrel, uhf; sirolimus, paclitaxel; true anaphylaxis after prior exposure to contrast media.
Description

ID.12

Data type

boolean

Alias
UMLS CUI [1]
C0020517
pregnancy (present, suspected or planned).
Description

ID.13

Data type

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0425965
patient's inability to fully cooperate with the study protocol.
Description

ID.14

Data type

boolean

Alias
UMLS CUI [1]
C1321605
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Similar models

Eligibility Coronary Disease NCT00598637

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
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])
ID.2
Item
pretreatment with a loading dose of 600 mg clopidogrel.
boolean
C0070166 (UMLS CUI [1,1])
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])
Item Group
C0680251 (UMLS CUI)
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])
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])
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])
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])
ID.14
Item
patient's inability to fully cooperate with the study protocol.
boolean
C1321605 (UMLS CUI [1])
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