Informationen:
Fehler:
ID
28578
Beschreibung
Clopidogrel and Response Variability Investigation Study 2; ODM derived from: https://clinicaltrials.gov/show/NCT00822666
Link
https://clinicaltrials.gov/show/NCT00822666
Stichworte
Versionen (1)
- 22.01.18 22.01.18 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
22. Januar 2018
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY 4.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Eligibility Coronary Artery Disease NCT00822666
Eligibility Coronary Artery Disease NCT00822666
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Coronary Artery Disease NCT00822666
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Age
Item
age > 18
boolean
C0001779 (UMLS CUI [1])
Gender
Item
male gender
boolean
C0079399 (UMLS CUI [1])
Patient Included Other Coding Registry
Item
included in the afiji registry
boolean
C0030705 (UMLS CUI [1,1])
C0332257 (UMLS CUI [1,2])
C3846158 (UMLS CUI [1,3])
C0034975 (UMLS CUI [1,4])
C0332257 (UMLS CUI [1,2])
C3846158 (UMLS CUI [1,3])
C0034975 (UMLS CUI [1,4])
High risk of bleeding Profile Absent
Item
no high bleeding risk profile
boolean
C4039184 (UMLS CUI [1,1])
C1979963 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C1979963 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Acute Coronary Syndrome Absent
Item
no recent history of acute coronary syndrome (< 3 months)
boolean
C0948089 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Informed Consent
Item
written informed consent obtained
boolean
C0021430 (UMLS CUI [1])
CYP2C19 Genotype | CYP2C19*1/*1 | CYP2C19*1/*2 | CYP2C19*2/*2
Item
genotype cyp2c19 : *1/*1, *1/*2 ou *2/*2
boolean
C1332828 (UMLS CUI [1,1])
C0017431 (UMLS CUI [1,2])
C3844564 (UMLS CUI [2])
C3844563 (UMLS CUI [3])
C3844561 (UMLS CUI [4])
C0017431 (UMLS CUI [1,2])
C3844564 (UMLS CUI [2])
C3844563 (UMLS CUI [3])
C3844561 (UMLS CUI [4])
P2Y12 Genotype | Other Coding
Item
genotype p2y12 : h1/h1 ou h1/h2
boolean
C1425330 (UMLS CUI [1,1])
C0017431 (UMLS CUI [1,2])
C3846158 (UMLS CUI [2])
C0017431 (UMLS CUI [1,2])
C3846158 (UMLS CUI [2])
Gender
Item
female gender
boolean
C0079399 (UMLS CUI [1])
Medical contraindication Clopidogrel
Item
patient with a contraindication to clopidogrel
boolean
C1301624 (UMLS CUI [1,1])
C0070166 (UMLS CUI [1,2])
C0070166 (UMLS CUI [1,2])
Clopidogrel Loading dose
Item
patient who has received a loading dose of clopidogrel in the past 7 days
boolean
C0070166 (UMLS CUI [1,1])
C3714444 (UMLS CUI [1,2])
C3714444 (UMLS CUI [1,2])
Ticlopidine | Platelet Glycoprotein IIb/IIIA Inhibitors
Item
patient treated with ticlopidine or gp2b/3a receptor antagonist prior to loading
boolean
C0040207 (UMLS CUI [1])
C1373125 (UMLS CUI [2])
C1373125 (UMLS CUI [2])
Compliance behavior Lacking
Item
non compliance
boolean
C1321605 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,2])
P2Y12 Genotype | Other Coding
Item
génotype p2y12 : h2/h2.
boolean
C1425330 (UMLS CUI [1,1])
C0017431 (UMLS CUI [1,2])
C3846158 (UMLS CUI [2])
C0017431 (UMLS CUI [1,2])
C3846158 (UMLS CUI [2])
Pharmaceutical Preparations Interaction Platelet aggregation | NSAIDs | Persantine | Serotonin Inhibitors
Item
patient treated with drugs interacting with platelet aggregation (nsaid, persantine, serotonin inhibitors )
boolean
C0013227 (UMLS CUI [1,1])
C0687133 (UMLS CUI [1,2])
C0032176 (UMLS CUI [1,3])
C0003211 (UMLS CUI [2])
C0700020 (UMLS CUI [3])
C0162758 (UMLS CUI [4])
C0687133 (UMLS CUI [1,2])
C0032176 (UMLS CUI [1,3])
C0003211 (UMLS CUI [2])
C0700020 (UMLS CUI [3])
C0162758 (UMLS CUI [4])
Pharmaceutical Preparations Interaction CYP2C19
Item
patient treated with drugs interacting 2c19
boolean
C0013227 (UMLS CUI [1,1])
C0687133 (UMLS CUI [1,2])
C0960580 (UMLS CUI [1,3])
C0687133 (UMLS CUI [1,2])
C0960580 (UMLS CUI [1,3])
National Health Insurance Affiliation Absent
Item
not affiliated to the national health insurance
boolean
C0027452 (UMLS CUI [1,1])
C1510825 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C1510825 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Study Subject Participation Status
Item
patient participating to another randomized study
boolean
C2348568 (UMLS CUI [1])