ID

21532

Description

Effect of Different Dosing Regimens of Clopidogrel Before Elective Percutaneous Coronary Intervention (PCI) on Platelet Function; ODM derived from: https://clinicaltrials.gov/show/NCT00693069

Lien

https://clinicaltrials.gov/show/NCT00693069

Mots-clés

  1. 26/04/2017 26/04/2017 -
Téléchargé le

26 avril 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Coronary Artery Disease NCT00693069

Eligibility Coronary Artery Disease NCT00693069

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult patient with an indication for elective coronary angiography with or without pci
Description

ID.1

Type de données

boolean

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0085532
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
major hemorrhagic diathesis or active bleeding
Description

ID.2

Type de données

boolean

Alias
UMLS CUI [1,1]
C0019087
UMLS CUI [1,2]
C0741554
acute myocardial infarction (mi) within 14 days of enrolment
Description

ID.3

Type de données

boolean

Alias
UMLS CUI [1]
C0155626
unstable angina with st-segment changes >1 mm in at least two contiguous electrocardiographic leads at rest or a troponin i level >0.06 microg/l within 14 days of enrolment
Description

ID.4

Type de données

boolean

Alias
UMLS CUI [1,1]
C0002965
UMLS CUI [1,2]
C0920117
UMLS CUI [1,3]
C0883409
stroke within the past 3 months
Description

ID.5

Type de données

boolean

Alias
UMLS CUI [1]
C0038454
platelet count <100 x 10 9/l
Description

ID.6

Type de données

boolean

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

ID.7

Type de données

boolean

Alias
UMLS CUI [1]
C0491338
hematocrit <25% or hemoglobin level <100 g/l
Description

ID.8

Type de données

boolean

Alias
UMLS CUI [1,1]
C0518014
UMLS CUI [1,2]
C0019046
alcohol or drug abuse
Description

ID.9

Type de données

boolean

Alias
UMLS CUI [1,1]
C0085762
UMLS CUI [1,2]
C0013146
enrolment in other investigational drug trials within the previous month
Description

ID.10

Type de données

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C4041024
use of thienopyridines, glycoprotein (gp) iib/iiia inhibitors, warfarin or acenocoumarol within the previous week
Description

ID.11

Type de données

boolean

Alias
UMLS CUI [1]
C2347852
allergic reaction or any contraindication to clopidogrel or aspirin administration
Description

ID.12

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0070166
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0004057

Similar models

Eligibility Coronary Artery Disease NCT00693069

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
adult patient with an indication for elective coronary angiography with or without pci
boolean
C0392360 (UMLS CUI [1,1])
C0085532 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
ID.2
Item
major hemorrhagic diathesis or active bleeding
boolean
C0019087 (UMLS CUI [1,1])
C0741554 (UMLS CUI [1,2])
ID.3
Item
acute myocardial infarction (mi) within 14 days of enrolment
boolean
C0155626 (UMLS CUI [1])
ID.4
Item
unstable angina with st-segment changes >1 mm in at least two contiguous electrocardiographic leads at rest or a troponin i level >0.06 microg/l within 14 days of enrolment
boolean
C0002965 (UMLS CUI [1,1])
C0920117 (UMLS CUI [1,2])
C0883409 (UMLS CUI [1,3])
ID.5
Item
stroke within the past 3 months
boolean
C0038454 (UMLS CUI [1])
ID.6
Item
platelet count <100 x 10 9/l
boolean
C0032181 (UMLS CUI [1])
ID.7
Item
prothrombin time > 1.5 times control
boolean
C0491338 (UMLS CUI [1])
ID.8
Item
hematocrit <25% or hemoglobin level <100 g/l
boolean
C0518014 (UMLS CUI [1,1])
C0019046 (UMLS CUI [1,2])
ID.9
Item
alcohol or drug abuse
boolean
C0085762 (UMLS CUI [1,1])
C0013146 (UMLS CUI [1,2])
ID.10
Item
enrolment in other investigational drug trials within the previous month
boolean
C2348568 (UMLS CUI [1,1])
C4041024 (UMLS CUI [1,2])
ID.11
Item
use of thienopyridines, glycoprotein (gp) iib/iiia inhibitors, warfarin or acenocoumarol within the previous week
boolean
C2347852 (UMLS CUI [1])
ID.12
Item
allergic reaction or any contraindication to clopidogrel or aspirin administration
boolean
C0020517 (UMLS CUI [1,1])
C0070166 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0004057 (UMLS CUI [2,2])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial