ID

20269

Description

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

Lien

https://clinicaltrials.gov/show/NCT00302913

Mots-clés

  1. 18/02/2017 18/02/2017 -
Téléchargé le

18 février 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT00302913

Eligibility Coronary Artery Disease NCT00302913

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients undergoing elective coronary stenting
Description

Coronary stenting elective

Type de données

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
Description

Clopidogrel Bolus dose | Coronary artery stent Implantation

Type de données

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
Description

Aspirin U/day

Type de données

boolean

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

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
written consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

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

Troponin T

Type de données

boolean

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

Myocardial Infarction | Thrombolytic Therapy

Type de données

boolean

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

Shock, Cardiogenic

Type de données

boolean

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

Medical contraindication Aspirin | Medical contraindication clopidogrel

Type de données

boolean

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

Anticoagulation Oral

Type de données

boolean

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

Heparin | thienopyridine

Type de données

boolean

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

GPIIb-IIIa receptor antagonists | Percutaneous Coronary Intervention

Type de données

boolean

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

Platelet Count measurement

Type de données

boolean

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

Blood Coagulation Disorders Severe

Type de données

boolean

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

Liver Dysfunction Severe | Renal alteration Severe

Type de données

boolean

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

Malignant Neoplasms

Type de données

boolean

Alias
UMLS CUI [1]
C0006826

Similar models

Eligibility Coronary Artery Disease NCT00302913

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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