ID

20269

Descripción

Efficacy of Adjusted Clopidogrel Dose in Patients With Insufficient Platelet Inhibition; ODM derived from: https://clinicaltrials.gov/show/NCT00302913

Link

https://clinicaltrials.gov/show/NCT00302913

Palabras clave

Versiones (1)
  1. 18/2/17 18/2/17 -
Subido en

18 de febrero de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT00302913

Inglés

Eligibility Coronary Artery Disease NCT00302913

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients undergoing elective coronary stenting
Descripción

Coronary stenting elective

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1272587
UMLS CUI [1,2]
C0439608
pretreatment with a bolus dose of 600mg of clopidogrel at least 2 hours prior to coronary stent implantation
Descripción

Clopidogrel Bolus dose | Coronary artery stent Implantation

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0070166
UMLS CUI [1,2]
C1511237
UMLS CUI [2,1]
C0687568
UMLS CUI [2,2]
C0021107
pretreatment with aspirin ≥ 100 mg per day for at least 7 days
Descripción

Aspirin U/day

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0004057
UMLS CUI [1,2]
C0456683
age > 18 years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
written consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

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

Troponin T

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0077404
myocardial infarction or fibrinolytic therapy within the previous 14 days
Descripción

Myocardial Infarction | Thrombolytic Therapy

Tipo de datos

boolean

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

Shock, Cardiogenic

Tipo de datos

boolean

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

Medical contraindication Aspirin | Medical contraindication clopidogrel

Tipo de datos

boolean

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

Anticoagulation Oral

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0003281
UMLS CUI [1,2]
C1527415
pretreatment with heparin or a thienopyridine within the previous 14 days
Descripción

Heparin | thienopyridine

Tipo de datos

boolean

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

GPIIb-IIIa receptor antagonists | Percutaneous Coronary Intervention

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0016011
UMLS CUI [1,2]
C0003139
UMLS CUI [2]
C1532338
platelet count < 100.000/µl
Descripción

Platelet Count measurement

Tipo de datos

boolean

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

Blood Coagulation Disorders Severe

Tipo de datos

boolean

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

Liver Dysfunction Severe | Renal alteration Severe

Tipo de datos

boolean

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

Malignant Neoplasms

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006826
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Similar models

Eligibility Coronary Artery Disease NCT00302913

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Coronary stenting elective
Item
patients undergoing elective coronary stenting
boolean
C1272587 (UMLS CUI [1,1])
C0439608 (UMLS CUI [1,2])
Clopidogrel Bolus dose | Coronary artery stent Implantation
Item
pretreatment with a bolus dose of 600mg of clopidogrel at least 2 hours prior to coronary stent implantation
boolean
C0070166 (UMLS CUI [1,1])
C1511237 (UMLS CUI [1,2])
C0687568 (UMLS CUI [2,1])
C0021107 (UMLS CUI [2,2])
Aspirin U/day
Item
pretreatment with aspirin ≥ 100 mg per day for at least 7 days
boolean
C0004057 (UMLS CUI [1,1])
C0456683 (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
Item
troponin t on admission > 0.03 ng/ml
boolean
C0077404 (UMLS CUI [1])
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])
Anticoagulation Oral
Item
oral anticoagulation
boolean
C0003281 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
Heparin | thienopyridine
Item
pretreatment with heparin or a thienopyridine within the previous 14 days
boolean
C0019134 (UMLS CUI [1])
C1120149 (UMLS CUI [2])
GPIIb-IIIa receptor antagonists | Percutaneous Coronary Intervention
Item
use of a gp iib/iiia-receptor antagonist during pci
boolean
C0016011 (UMLS CUI [1,1])
C0003139 (UMLS CUI [1,2])
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 Neoplasms
Item
cancer
boolean
C0006826 (UMLS CUI [1])
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