Englisch

Eligibility Coronary Artery Disease NCT00428454

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
the estimated duration of the occlusion is at least 2 weeks.
Beschreibung

Occlusion Duration Estimated

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1947917
UMLS CUI [1,2]
C0449238
UMLS CUI [1,3]
C0750572
signs of ischemia related to the occluded coronary artery.
Beschreibung

Signs Ischemia | Relationship Coronary Occlusion

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0311392
UMLS CUI [1,2]
C0022116
UMLS CUI [2,1]
C0439849
UMLS CUI [2,2]
C0151814
successful recanalization of the occluded artery is achieved.
Beschreibung

Coronary Occlusion Recanalization Successful

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0151814
UMLS CUI [1,2]
C0034771
UMLS CUI [1,3]
C1272703
reference diameter is > 2.5 mm.
Beschreibung

Reference Diameter Size

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1706462
UMLS CUI [1,2]
C1301886
UMLS CUI [1,3]
C0456389
written informed consent obtained.
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
primary or rescue pci for acute myocardial infarction
Beschreibung

Percutaneous Coronary Intervention Primary Myocardial Infarction | Emergency Percutaneous Coronary Intervention Myocardial Infarction

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0205225
UMLS CUI [1,3]
C0027051
UMLS CUI [2,1]
C0013956
UMLS CUI [2,2]
C1532338
UMLS CUI [2,3]
C0027051
the lesion could not be crossed.
Beschreibung

Lesion Crossed Unsuccessful

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0205203
UMLS CUI [1,3]
C1272705
lesions with complex anatomy making successful stent deployment unlikely.
Beschreibung

Lesion Anatomy Complex | Placement of stent Unlikely

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0700276
UMLS CUI [1,3]
C0439855
UMLS CUI [2,1]
C0522776
UMLS CUI [2,2]
C0750558
the guide wire is not in the true lumen distal to the occlusion.
Beschreibung

Guide wire Lumen Relationship Inappropriate | Lumen Distal Occlusion

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0181089
UMLS CUI [1,2]
C0225997
UMLS CUI [1,3]
C0439849
UMLS CUI [1,4]
C1548788
UMLS CUI [2,1]
C0225997
UMLS CUI [2,2]
C0205108
UMLS CUI [2,3]
C1947917
sirolimus or zotarolimus allergy
Beschreibung

Hypersensitivity Sirolimus | Hypersensitivity Zotarolimus

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0072980
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C1700035
venous or arterial bypass grafts
Beschreibung

Vein Bypass Graft Procedures | Bypass graft Arterial

Datentyp

boolean

Alias
UMLS CUI [1]
C0519413
UMLS CUI [2,1]
C0185098
UMLS CUI [2,2]
C0221464
pregnant or nursing women.
Beschreibung

Pregnancy | Breast Feeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
participation in an other trial.
Beschreibung

Study Subject Participation Status

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
factors making long-term follow-up difficult or unlikely.
Beschreibung

Factor Long-term Follow-up Difficult | Factor Long-term Follow-up Unlikely

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1521761
UMLS CUI [1,2]
C1517942
UMLS CUI [1,3]
C0332218
UMLS CUI [2,1]
C1521761
UMLS CUI [2,2]
C1517942
UMLS CUI [2,3]
C0750558
life expectancy <1 year.
Beschreibung

Life Expectancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0023671
contraindications for asa or clopidogrel or heparin.
Beschreibung

Medical contraindication Aspirin | Medical contraindication Clopidogrel | Medical contraindication Heparin

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0004057
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0070166
UMLS CUI [3,1]
C1301624
UMLS CUI [3,2]
C0019134
use of coumadins that could not be stopped before the procedure.
Beschreibung

Coumadin Discontinuation Unsuccessful

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0699129
UMLS CUI [1,2]
C1444662
UMLS CUI [1,3]
C1272705
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Ähnliche Modelle

Eligibility Coronary Artery Disease NCT00428454

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Occlusion Duration Estimated
Item
the estimated duration of the occlusion is at least 2 weeks.
boolean
C1947917 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0750572 (UMLS CUI [1,3])
Signs Ischemia | Relationship Coronary Occlusion
Item
signs of ischemia related to the occluded coronary artery.
boolean
C0311392 (UMLS CUI [1,1])
C0022116 (UMLS CUI [1,2])
C0439849 (UMLS CUI [2,1])
C0151814 (UMLS CUI [2,2])
Coronary Occlusion Recanalization Successful
Item
successful recanalization of the occluded artery is achieved.
boolean
C0151814 (UMLS CUI [1,1])
C0034771 (UMLS CUI [1,2])
C1272703 (UMLS CUI [1,3])
Reference Diameter Size
Item
reference diameter is > 2.5 mm.
boolean
C1706462 (UMLS CUI [1,1])
C1301886 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,3])
Informed Consent
Item
written informed consent obtained.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Percutaneous Coronary Intervention Primary Myocardial Infarction | Emergency Percutaneous Coronary Intervention Myocardial Infarction
Item
primary or rescue pci for acute myocardial infarction
boolean
C1532338 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0027051 (UMLS CUI [1,3])
C0013956 (UMLS CUI [2,1])
C1532338 (UMLS CUI [2,2])
C0027051 (UMLS CUI [2,3])
Lesion Crossed Unsuccessful
Item
the lesion could not be crossed.
boolean
C0221198 (UMLS CUI [1,1])
C0205203 (UMLS CUI [1,2])
C1272705 (UMLS CUI [1,3])
Lesion Anatomy Complex | Placement of stent Unlikely
Item
lesions with complex anatomy making successful stent deployment unlikely.
boolean
C0221198 (UMLS CUI [1,1])
C0700276 (UMLS CUI [1,2])
C0439855 (UMLS CUI [1,3])
C0522776 (UMLS CUI [2,1])
C0750558 (UMLS CUI [2,2])
Guide wire Lumen Relationship Inappropriate | Lumen Distal Occlusion
Item
the guide wire is not in the true lumen distal to the occlusion.
boolean
C0181089 (UMLS CUI [1,1])
C0225997 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C1548788 (UMLS CUI [1,4])
C0225997 (UMLS CUI [2,1])
C0205108 (UMLS CUI [2,2])
C1947917 (UMLS CUI [2,3])
Hypersensitivity Sirolimus | Hypersensitivity Zotarolimus
Item
sirolimus or zotarolimus allergy
boolean
C0020517 (UMLS CUI [1,1])
C0072980 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C1700035 (UMLS CUI [2,2])
Vein Bypass Graft Procedures | Bypass graft Arterial
Item
venous or arterial bypass grafts
boolean
C0519413 (UMLS CUI [1])
C0185098 (UMLS CUI [2,1])
C0221464 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
pregnant or nursing women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status
Item
participation in an other trial.
boolean
C2348568 (UMLS CUI [1])
Factor Long-term Follow-up Difficult | Factor Long-term Follow-up Unlikely
Item
factors making long-term follow-up difficult or unlikely.
boolean
C1521761 (UMLS CUI [1,1])
C1517942 (UMLS CUI [1,2])
C0332218 (UMLS CUI [1,3])
C1521761 (UMLS CUI [2,1])
C1517942 (UMLS CUI [2,2])
C0750558 (UMLS CUI [2,3])
Life Expectancy
Item
life expectancy <1 year.
boolean
C0023671 (UMLS CUI [1])
Medical contraindication Aspirin | Medical contraindication Clopidogrel | Medical contraindication Heparin
Item
contraindications for asa or clopidogrel or heparin.
boolean
C1301624 (UMLS CUI [1,1])
C0004057 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
C1301624 (UMLS CUI [3,1])
C0019134 (UMLS CUI [3,2])
Coumadin Discontinuation Unsuccessful
Item
use of coumadins that could not be stopped before the procedure.
boolean
C0699129 (UMLS CUI [1,1])
C1444662 (UMLS CUI [1,2])
C1272705 (UMLS CUI [1,3])
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