ID

16940

Descripción

H2 Haplotype and CYP3As Polymorphisms and the Antiplatelet Response to Clopidogrel; ODM derived from: https://clinicaltrials.gov/show/NCT00433784

Link

https://clinicaltrials.gov/show/NCT00433784

Palabras clave

Versiones (1)
  1. 15/8/16 15/8/16 -
Subido en

15 de agosto de 2016

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT00433784

Inglés

Eligibility Coronary Artery Disease NCT00433784

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
documented coronary artery disease (cad) requiring an elective diagnostic coronary angiography with or without percutaneous coronary intervention (pci)
Descripción

Coronary Artery Disease Requirement Coronary angiography elective | Percutaneous Coronary Intervention

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1956346
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0085532
UMLS CUI [1,4]
C0439608
UMLS CUI [2]
C1532338
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
major bleeding disorders or active bleeding;
Descripción

Blood Coagulation Disorders Major | Hemorrhage

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0005779
UMLS CUI [1,2]
C0205164
UMLS CUI [2]
C0019080
acute mi within 14 days of recruitment;
Descripción

Acute myocardial infarction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0155626
unstable angina with st-segment changes of > or = 1 mm in at least two contiguous electrocardiographic leads at rest, a troponin level of > 0.06 ug/l or both within 14 days of recruitment;
Descripción

Angina, Unstable | EKG ST segment changes | 12 lead electrocardiogram at rest Quantity | Troponin measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0002965
UMLS CUI [2]
C0232326
UMLS CUI [3,1]
C2960418
UMLS CUI [3,2]
C1265611
UMLS CUI [4]
C0523952
stroke within the last 3 months;
Descripción

Cerebrovascular accident

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038454
platelet count < 100 x 109/l;
Descripción

Platelet Count measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032181
prothrombin time > 1.5 times control;
Descripción

Prothrombin time assay

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0033707
hematocrit < 25% or hemoglobin level < 100 g/l;
Descripción

Hematocrit level | Hemoglobin concentration result

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0518014
UMLS CUI [2]
C0019029
alcohol or drug abuse;
Descripción

Substance Use Disorders

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038586
enrolment in other investigational drug trials within the previous month;
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
use of thienopyridines, glycoprotein (gp) iib/iiia inhibitors, warfarin or acenocoumarol within the prior week;
Descripción

Thienopyridines | Platelet Glycoprotein IIb/IIIA Inhibitors | Warfarin | Acenocoumarol

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2936588
UMLS CUI [2]
C1373125
UMLS CUI [3]
C0043031
UMLS CUI [4]
C0000956
allergic reaction or any contraindication to clopidogrel or aspirin.
Descripción

Allergic Reaction clopidogrel | Medical contraindication clopidogrel | Allergic Reaction Aspirin | Medical contraindication Aspirin

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1527304
UMLS CUI [1,2]
C0070166
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0070166
UMLS CUI [3,1]
C1527304
UMLS CUI [3,2]
C0004057
UMLS CUI [4,1]
C1301624
UMLS CUI [4,2]
C0004057
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Similar models

Eligibility Coronary Artery Disease NCT00433784

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Coronary Artery Disease Requirement Coronary angiography elective | Percutaneous Coronary Intervention
Item
documented coronary artery disease (cad) requiring an elective diagnostic coronary angiography with or without percutaneous coronary intervention (pci)
boolean
C1956346 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0085532 (UMLS CUI [1,3])
C0439608 (UMLS CUI [1,4])
C1532338 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Blood Coagulation Disorders Major | Hemorrhage
Item
major bleeding disorders or active bleeding;
boolean
C0005779 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C0019080 (UMLS CUI [2])
Acute myocardial infarction
Item
acute mi within 14 days of recruitment;
boolean
C0155626 (UMLS CUI [1])
Angina, Unstable | EKG ST segment changes | 12 lead electrocardiogram at rest Quantity | Troponin measurement
Item
unstable angina with st-segment changes of > or = 1 mm in at least two contiguous electrocardiographic leads at rest, a troponin level of > 0.06 ug/l or both within 14 days of recruitment;
boolean
C0002965 (UMLS CUI [1])
C0232326 (UMLS CUI [2])
C2960418 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C0523952 (UMLS CUI [4])
Cerebrovascular accident
Item
stroke within the last 3 months;
boolean
C0038454 (UMLS CUI [1])
Platelet Count measurement
Item
platelet count < 100 x 109/l;
boolean
C0032181 (UMLS CUI [1])
Prothrombin time assay
Item
prothrombin time > 1.5 times control;
boolean
C0033707 (UMLS CUI [1])
Hematocrit level | Hemoglobin concentration result
Item
hematocrit < 25% or hemoglobin level < 100 g/l;
boolean
C0518014 (UMLS CUI [1])
C0019029 (UMLS CUI [2])
Substance Use Disorders
Item
alcohol or drug abuse;
boolean
C0038586 (UMLS CUI [1])
Study Subject Participation Status
Item
enrolment in other investigational drug trials within the previous month;
boolean
C2348568 (UMLS CUI [1])
Thienopyridines | Platelet Glycoprotein IIb/IIIA Inhibitors | Warfarin | Acenocoumarol
Item
use of thienopyridines, glycoprotein (gp) iib/iiia inhibitors, warfarin or acenocoumarol within the prior week;
boolean
C2936588 (UMLS CUI [1])
C1373125 (UMLS CUI [2])
C0043031 (UMLS CUI [3])
C0000956 (UMLS CUI [4])
Allergic Reaction clopidogrel | Medical contraindication clopidogrel | Allergic Reaction Aspirin | Medical contraindication Aspirin
Item
allergic reaction or any contraindication to clopidogrel or aspirin.
boolean
C1527304 (UMLS CUI [1,1])
C0070166 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
C1527304 (UMLS CUI [3,1])
C0004057 (UMLS CUI [3,2])
C1301624 (UMLS CUI [4,1])
C0004057 (UMLS CUI [4,2])
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