ID

16943

Beschrijving

Effect of Clopidogrel Loading and Risk of PCI; ODM derived from: https://clinicaltrials.gov/show/NCT00457236

Link

https://clinicaltrials.gov/show/NCT00457236

Trefwoorden

  1. 15-08-16 15-08-16 -
Geüploaded op

15 augustus 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT00457236

Eligibility Coronary Artery Disease NCT00457236

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients undergoing elective coronary stenting
Beschrijving

Coronary artery stent elective

Datatype

boolean

Alias
UMLS CUI [1,1]
C0687568
UMLS CUI [1,2]
C0439608
pretreatment with a bolus dose of 600mg of clopidogrel prior to coronary stent implantation
Beschrijving

Pretreatment clopidogrel bolus infusion | Placement of stent in coronary artery

Datatype

boolean

Alias
UMLS CUI [1,1]
C3539076
UMLS CUI [1,2]
C0070166
UMLS CUI [1,3]
C1511237
UMLS CUI [2]
C0521232
pretreatment with aspirin ≥ 100 mg per day for at least 7 days
Beschrijving

Pretreatment Aspirin

Datatype

boolean

Alias
UMLS CUI [1,1]
C3539076
UMLS CUI [1,2]
C0004057
age > 18 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
written consent
Beschrijving

Informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
troponin t on admission > 0.03 ng/ml
Beschrijving

Troponin T On admission

Datatype

boolean

Alias
UMLS CUI [1,1]
C0077404
UMLS CUI [1,2]
C0457453
myocardial infarction or fibrinolytic therapy within the previous 14 days
Beschrijving

Myocardial Infarction | Thrombolytic Therapy

Datatype

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0040044
cardiogenic shock
Beschrijving

Shock, Cardiogenic

Datatype

boolean

Alias
UMLS CUI [1]
C0036980
contraindication for aspirin or clopidogrel
Beschrijving

Medical contraindication Aspirin | Medical contraindication clopidogrel

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0004057
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0070166
oral anticoagulation
Beschrijving

oral anticoagulants

Datatype

boolean

Alias
UMLS CUI [1]
C0354604
pretreatment with heparin or a thienopyridine within the previous 14 days
Beschrijving

Pretreatment Heparin | Pretreatment thienopyridine

Datatype

boolean

Alias
UMLS CUI [1,1]
C3539076
UMLS CUI [1,2]
C0019134
UMLS CUI [2,1]
C3539076
UMLS CUI [2,2]
C1120149
use of a gp iib/iiia-receptor antagonist during pci
Beschrijving

Glycoprotein IIb/IIIa Antagonist | Percutaneous Coronary Intervention

Datatype

boolean

Alias
UMLS CUI [1]
C3640054
UMLS CUI [2]
C1532338
platelet count < 100.000/µl
Beschrijving

Platelet Count measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0032181
severe disorders of the coagulation system
Beschrijving

Blood Coagulation Disorders Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C0005779
UMLS CUI [1,2]
C0205082
severe impairment of liver or kidney function
Beschrijving

Liver Dysfunction Severe | Renal alteration Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C0086565
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0184571
UMLS CUI [2,2]
C0205082
cancer
Beschrijving

Malignant Neoplasm

Datatype

boolean

Alias
UMLS CUI [1]
C0006826

Similar models

Eligibility Coronary Artery Disease NCT00457236

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Coronary artery stent elective
Item
patients undergoing elective coronary stenting
boolean
C0687568 (UMLS CUI [1,1])
C0439608 (UMLS CUI [1,2])
Pretreatment clopidogrel bolus infusion | Placement of stent in coronary artery
Item
pretreatment with a bolus dose of 600mg of clopidogrel prior to coronary stent implantation
boolean
C3539076 (UMLS CUI [1,1])
C0070166 (UMLS CUI [1,2])
C1511237 (UMLS CUI [1,3])
C0521232 (UMLS CUI [2])
Pretreatment Aspirin
Item
pretreatment with aspirin ≥ 100 mg per day for at least 7 days
boolean
C3539076 (UMLS CUI [1,1])
C0004057 (UMLS CUI [1,2])
Age
Item
age > 18 years
boolean
C0001779 (UMLS CUI [1])
Informed consent
Item
written consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Troponin T On admission
Item
troponin t on admission > 0.03 ng/ml
boolean
C0077404 (UMLS CUI [1,1])
C0457453 (UMLS CUI [1,2])
Myocardial Infarction | Thrombolytic Therapy
Item
myocardial infarction or fibrinolytic therapy within the previous 14 days
boolean
C0027051 (UMLS CUI [1])
C0040044 (UMLS CUI [2])
Shock, Cardiogenic
Item
cardiogenic shock
boolean
C0036980 (UMLS CUI [1])
Medical contraindication Aspirin | Medical contraindication clopidogrel
Item
contraindication for aspirin or clopidogrel
boolean
C1301624 (UMLS CUI [1,1])
C0004057 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
oral anticoagulants
Item
oral anticoagulation
boolean
C0354604 (UMLS CUI [1])
Pretreatment Heparin | Pretreatment thienopyridine
Item
pretreatment with heparin or a thienopyridine within the previous 14 days
boolean
C3539076 (UMLS CUI [1,1])
C0019134 (UMLS CUI [1,2])
C3539076 (UMLS CUI [2,1])
C1120149 (UMLS CUI [2,2])
Glycoprotein IIb/IIIa Antagonist | Percutaneous Coronary Intervention
Item
use of a gp iib/iiia-receptor antagonist during pci
boolean
C3640054 (UMLS CUI [1])
C1532338 (UMLS CUI [2])
Platelet Count measurement
Item
platelet count < 100.000/µl
boolean
C0032181 (UMLS CUI [1])
Blood Coagulation Disorders Severe
Item
severe disorders of the coagulation system
boolean
C0005779 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Liver Dysfunction Severe | Renal alteration Severe
Item
severe impairment of liver or kidney function
boolean
C0086565 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0184571 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Malignant Neoplasm
Item
cancer
boolean
C0006826 (UMLS CUI [1])

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