ID

28715

Descripción

The EFFect of hIgh Dose ClopIdogrel treatmENT in Patients With Clopidogrel Resistance; ODM derived from: https://clinicaltrials.gov/show/NCT01032668

Link

https://clinicaltrials.gov/show/NCT01032668

Palabras clave

Versiones (1)
  1. 26/1/18 26/1/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

26 de enero de 2018

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT01032668

Inglés

Eligibility Coronary Artery Disease NCT01032668

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
the patients; who have planned elective pci and have had written informed consent for participation to study.
Descripción

Percutaneous Coronary Intervention elective Planned | Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0439608
UMLS CUI [1,3]
C1301732
UMLS CUI [2]
C0021430
age>18 year-old,
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
the native coronary artery;lesion with narrowing >=70%
Descripción

Coronary artery Native | Lesion Stenosis Percentage

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0205042
UMLS CUI [1,2]
C0302891
UMLS CUI [2,1]
C0221198
UMLS CUI [2,2]
C1261287
UMLS CUI [2,3]
C0439165
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients have allergy for asa, clopidogrel and heparin
Descripción

Aspirin allergy | Hypersensitivity clopidogrel | Heparin allergy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004058
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0070166
UMLS CUI [3]
C0571776
patients who performed primary pci
Descripción

Percutaneous Coronary Intervention Primary

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0205225
patients with acute coronary syndrome
Descripción

Acute Coronary Syndrome

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0948089
patients with have a history of pci and use clopidogrel
Descripción

History Percutaneous Coronary Intervention | Clopidogrel Use of

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C1532338
UMLS CUI [2,1]
C0070166
UMLS CUI [2,2]
C1524063
patients on warfarin therapy
Descripción

Warfarin

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0043031
patients who have bleeding diathesis, or have high risk for bleeding.
Descripción

Bleeding tendency | High risk of bleeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1458140
UMLS CUI [2]
C4039184
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Similar models

Eligibility Coronary Artery Disease NCT01032668

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Percutaneous Coronary Intervention elective Planned | Informed Consent
Item
the patients; who have planned elective pci and have had written informed consent for participation to study.
boolean
C1532338 (UMLS CUI [1,1])
C0439608 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
C0021430 (UMLS CUI [2])
Age
Item
age>18 year-old,
boolean
C0001779 (UMLS CUI [1])
Coronary artery Native | Lesion Stenosis Percentage
Item
the native coronary artery;lesion with narrowing >=70%
boolean
C0205042 (UMLS CUI [1,1])
C0302891 (UMLS CUI [1,2])
C0221198 (UMLS CUI [2,1])
C1261287 (UMLS CUI [2,2])
C0439165 (UMLS CUI [2,3])
Item Group
C0680251 (UMLS CUI)
Aspirin allergy | Hypersensitivity clopidogrel | Heparin allergy
Item
patients have allergy for asa, clopidogrel and heparin
boolean
C0004058 (UMLS CUI [1])
C0020517 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
C0571776 (UMLS CUI [3])
Percutaneous Coronary Intervention Primary
Item
patients who performed primary pci
boolean
C1532338 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
Acute Coronary Syndrome
Item
patients with acute coronary syndrome
boolean
C0948089 (UMLS CUI [1])
History Percutaneous Coronary Intervention | Clopidogrel Use of
Item
patients with have a history of pci and use clopidogrel
boolean
C0262926 (UMLS CUI [1,1])
C1532338 (UMLS CUI [1,2])
C0070166 (UMLS CUI [2,1])
C1524063 (UMLS CUI [2,2])
Warfarin
Item
patients on warfarin therapy
boolean
C0043031 (UMLS CUI [1])
Bleeding tendency | High risk of bleeding
Item
patients who have bleeding diathesis, or have high risk for bleeding.
boolean
C1458140 (UMLS CUI [1])
C4039184 (UMLS CUI [2])
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