ID

12877

Beschrijving

EUropean Pharmacogenetics of AntiCoagulant Therapy - Acenocoumarol; ODM derived from: https://clinicaltrials.gov/show/NCT01119261

Link

https://clinicaltrials.gov/show/NCT01119261

Trefwoorden

  1. 04-01-16 04-01-16 -
Geüploaded op

4 januari 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Venous Thromboembolism NCT01119261

Eligibility Venous Thromboembolism NCT01119261

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with either venous thromboembolism (vte) or atrial fibrillation (af) requiring coumarin therapy for at least 12 weeks and a target inr in the low intensity range (inr range 2-3 in the united kingdom, sweden, germany, austria and greece and inr 2.5-3.5 in the netherlands)
Beschrijving

venous thromboembolism; atrial fibrillation; coumarin

Datatype

boolean

Alias
UMLS CUI [1]
C1861172
UMLS CUI [2]
C0004238
UMLS CUI [3]
C0010206
age ≥ 18 years
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
ability to attend scheduled visits
Beschrijving

compliance behavior

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
signed informed consent
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
presence of a mechanical heart valve
Beschrijving

mechanical heart valve

Datatype

boolean

Alias
UMLS CUI [1]
C0493527
severe cognitive impairment
Beschrijving

cognitive impairment

Datatype

boolean

Alias
UMLS CUI [1]
C1839000
known genotype cyp2c9 or vkorc1 at start of the study
Beschrijving

genotype CYP2 gene VKOR gene

Datatype

boolean

Alias
UMLS CUI [1,1]
C0017431
UMLS CUI [1,2]
C1332829
UMLS CUI [1,3]
C1428184
previous or current treatment with any coumarin
Beschrijving

therapy coumarin

Datatype

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0010206
pregnancy or lactation
Beschrijving

pregnancy; lactating

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
non-eligible subject
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Venous Thromboembolism NCT01119261

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
venous thromboembolism; atrial fibrillation; coumarin
Item
patients with either venous thromboembolism (vte) or atrial fibrillation (af) requiring coumarin therapy for at least 12 weeks and a target inr in the low intensity range (inr range 2-3 in the united kingdom, sweden, germany, austria and greece and inr 2.5-3.5 in the netherlands)
boolean
C1861172 (UMLS CUI [1])
C0004238 (UMLS CUI [2])
C0010206 (UMLS CUI [3])
age
Item
age ≥ 18 years
boolean
C0001779 (UMLS CUI [1])
compliance behavior
Item
ability to attend scheduled visits
boolean
C1321605 (UMLS CUI [1])
informed consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
mechanical heart valve
Item
presence of a mechanical heart valve
boolean
C0493527 (UMLS CUI [1])
cognitive impairment
Item
severe cognitive impairment
boolean
C1839000 (UMLS CUI [1])
genotype CYP2 gene VKOR gene
Item
known genotype cyp2c9 or vkorc1 at start of the study
boolean
C0017431 (UMLS CUI [1,1])
C1332829 (UMLS CUI [1,2])
C1428184 (UMLS CUI [1,3])
therapy coumarin
Item
previous or current treatment with any coumarin
boolean
C0087111 (UMLS CUI [1,1])
C0010206 (UMLS CUI [1,2])
pregnancy; lactating
Item
pregnancy or lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status
Item
non-eligible subject
boolean
C2348568 (UMLS CUI [1])

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