ID

16746

Beschrijving

Randomised Study Comparing Three Chemotherapy Regimens in Non-small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00622349

Link

https://clinicaltrials.gov/show/NCT00622349

Trefwoorden

  1. 03-08-16 03-08-16 -
Geüploaded op

3 augustus 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Carcinoma, Non-Small-Cell Lung NCT00622349

Eligibility Carcinoma, Non-Small-Cell Lung NCT00622349

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
histological or cytological diagnosis of non-small cell lung cancer
Beschrijving

diagnosis of non-small cell lung cancer

Datatype

boolean

Alias
UMLS CUI [1,1]
C0011900
UMLS CUI [1,2]
C0007131
advanced (unresectable or functionally inoperable) stage iii or stage iv disease
Beschrijving

Advanced disease

Datatype

boolean

Alias
UMLS CUI [1]
C0679246
availability for participating in the detailed follow-up of the protocol
Beschrijving

availability for follow-up

Datatype

boolean

Alias
UMLS CUI [1,1]
C0470187
UMLS CUI [1,2]
C1522577
presence of an evaluable or measurable lesion
Beschrijving

measurable disease

Datatype

boolean

Alias
UMLS CUI [1]
C1513041
informed consent
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior treatment with chemotherapy
Beschrijving

prior chemotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C1514457
operable patient with resectable tumor
Beschrijving

operability

Datatype

boolean

Alias
UMLS CUI [1]
C0205188
UMLS CUI [2,1]
C0027651
UMLS CUI [2,2]
C1514888
performance status < 60 on the karnofsky scale
Beschrijving

karnofsky performance status

Datatype

boolean

Alias
UMLS CUI [1]
C0206065
a history of prior malignant tumour, except non-melanoma skin cancer or in situ carcinoma of the cervix and cured malignant tumour (more than 5-year disease free interval)
Beschrijving

history of prior malignant tumour

Datatype

boolean

Alias
UMLS CUI [1]
C0260455
polynuclear cells < 2,000/mm³
Beschrijving

polynuclear cells

Datatype

boolean

platelet cells < 100,000/mm³
Beschrijving

blood platelets

Datatype

boolean

Alias
UMLS CUI [1]
C0005821
serum bilirubin >1.5 mg/100 ml
Beschrijving

serum bilirubin

Datatype

boolean

Alias
UMLS CUI [1]
C1278039
serum creatinine > 1.5 mg/100 ml and/or creatinine clearance < 60 ml/min
Beschrijving

serum creatinine

Datatype

boolean

Alias
UMLS CUI [1]
C0201976
perception hypoacusis
Beschrijving

perception hypoacusia

Datatype

boolean

Alias
UMLS CUI [1]
C1963781
peripheral neuropathy
Beschrijving

peripheral neuropathy

Datatype

boolean

Alias
UMLS CUI [1]
C0031117
recent myocardial infarction (less than 3 months prior to date of diagnosis)
Beschrijving

myocardial infarction

Datatype

boolean

Alias
UMLS CUI [1]
C0027051
congestive cardiac failure requiring medical therapy or uncontrolled cardiac arrhythmia
Beschrijving

congestive cardiac failure requiring medical therapy or uncontrolled cardiac arrhythmia

Datatype

boolean

Alias
UMLS CUI [1]
C0018802
UMLS CUI [2]
C0003811
uncontrolled infectious disease
Beschrijving

uncontrolled infectious disease

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C0205318
serious medical or psychological factors which may prevent adherence to the treatment schedule
Beschrijving

comorbidity, mental disorders, compliance

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
UMLS CUI [2]
C0004936
UMLS CUI [3]
C1321605

Similar models

Eligibility Carcinoma, Non-Small-Cell Lung NCT00622349

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
diagnosis of non-small cell lung cancer
Item
histological or cytological diagnosis of non-small cell lung cancer
boolean
C0011900 (UMLS CUI [1,1])
C0007131 (UMLS CUI [1,2])
Advanced disease
Item
advanced (unresectable or functionally inoperable) stage iii or stage iv disease
boolean
C0679246 (UMLS CUI [1])
availability for follow-up
Item
availability for participating in the detailed follow-up of the protocol
boolean
C0470187 (UMLS CUI [1,1])
C1522577 (UMLS CUI [1,2])
measurable disease
Item
presence of an evaluable or measurable lesion
boolean
C1513041 (UMLS CUI [1])
informed consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
prior chemotherapy
Item
prior treatment with chemotherapy
boolean
C1514457 (UMLS CUI [1])
operability
Item
operable patient with resectable tumor
boolean
C0205188 (UMLS CUI [1])
C0027651 (UMLS CUI [2,1])
C1514888 (UMLS CUI [2,2])
karnofsky performance status
Item
performance status < 60 on the karnofsky scale
boolean
C0206065 (UMLS CUI [1])
history of prior malignant tumour
Item
a history of prior malignant tumour, except non-melanoma skin cancer or in situ carcinoma of the cervix and cured malignant tumour (more than 5-year disease free interval)
boolean
C0260455 (UMLS CUI [1])
polynuclear cells
Item
polynuclear cells < 2,000/mm³
boolean
blood platelets
Item
platelet cells < 100,000/mm³
boolean
C0005821 (UMLS CUI [1])
serum bilirubin
Item
serum bilirubin >1.5 mg/100 ml
boolean
C1278039 (UMLS CUI [1])
serum creatinine
Item
serum creatinine > 1.5 mg/100 ml and/or creatinine clearance < 60 ml/min
boolean
C0201976 (UMLS CUI [1])
perception hypoacusia
Item
perception hypoacusis
boolean
C1963781 (UMLS CUI [1])
peripheral neuropathy
Item
peripheral neuropathy
boolean
C0031117 (UMLS CUI [1])
myocardial infarction
Item
recent myocardial infarction (less than 3 months prior to date of diagnosis)
boolean
C0027051 (UMLS CUI [1])
congestive cardiac failure requiring medical therapy or uncontrolled cardiac arrhythmia
Item
congestive cardiac failure requiring medical therapy or uncontrolled cardiac arrhythmia
boolean
C0018802 (UMLS CUI [1])
C0003811 (UMLS CUI [2])
uncontrolled infectious disease
Item
uncontrolled infectious disease
boolean
C0009450 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
comorbidity, mental disorders, compliance
Item
serious medical or psychological factors which may prevent adherence to the treatment schedule
boolean
C0009488 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
C1321605 (UMLS CUI [3])

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