ID

16023

Beschrijving

Patients Preference for Oral or i.v. Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT00212589

Link

https://clinicaltrials.gov/show/NCT00212589

Trefwoorden

  1. 26-06-16 26-06-16 -
Geüploaded op

26 juni 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Colorectal Cancer NCT00212589

Eligibility Colorectal Cancer NCT00212589

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
indication for treatment with a fu-regime
Beschrijving

indication for fluorouracil treatment

Datatype

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0016360
who performance status 0-1
Beschrijving

who performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1298650
life expectancy > 3 months
Beschrijving

life expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
adequate haematological, renal and hepatic functions
Beschrijving

haematological, renal and hepatic function

Datatype

boolean

Alias
UMLS CUI [1,1]
C0221130
UMLS CUI [1,2]
C0232804
UMLS CUI [1,3]
C0232741
adequate contraceptives
Beschrijving

contraception

Datatype

boolean

Alias
UMLS CUI [1]
C0700589
written informed consent
Beschrijving

written informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
known cns-metastases
Beschrijving

cns-metastases

Datatype

boolean

Alias
UMLS CUI [1]
C0686377
prior treatment with chemotherapy
Beschrijving

prior chemotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C1514457
pregnant or breast feeding women
Beschrijving

pregnant or lactating

Datatype

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
current infection, unresolved bowel obstruction or subobstruction, uncontrolled crohn's disease or ulcerative colitis
Beschrijving

current infection or bowel disease

Datatype

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0021843
UMLS CUI [3]
C0010346
UMLS CUI [4]
C0009324
other serious illness or medical conditions
Beschrijving

serious comorbidities

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205404

Similar models

Eligibility Colorectal Cancer NCT00212589

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
indication for fluorouracil treatment
Item
indication for treatment with a fu-regime
boolean
C0087111 (UMLS CUI [1,1])
C0016360 (UMLS CUI [1,2])
who performance status
Item
who performance status 0-1
boolean
C1298650 (UMLS CUI [1])
life expectancy
Item
life expectancy > 3 months
boolean
C0023671 (UMLS CUI [1])
haematological, renal and hepatic function
Item
adequate haematological, renal and hepatic functions
boolean
C0221130 (UMLS CUI [1,1])
C0232804 (UMLS CUI [1,2])
C0232741 (UMLS CUI [1,3])
contraception
Item
adequate contraceptives
boolean
C0700589 (UMLS CUI [1])
written informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
cns-metastases
Item
known cns-metastases
boolean
C0686377 (UMLS CUI [1])
prior chemotherapy
Item
prior treatment with chemotherapy
boolean
C1514457 (UMLS CUI [1])
pregnant or lactating
Item
pregnant or breast feeding women
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
current infection or bowel disease
Item
current infection, unresolved bowel obstruction or subobstruction, uncontrolled crohn's disease or ulcerative colitis
boolean
C0009450 (UMLS CUI [1])
C0021843 (UMLS CUI [2])
C0010346 (UMLS CUI [3])
C0009324 (UMLS CUI [4])
serious comorbidities
Item
other serious illness or medical conditions
boolean
C0009488 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])

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