ID

34428

Beschrijving

the Quality of Life Assessment of Advanced Non-small Cell Lung Cancer in China; ODM derived from: https://clinicaltrials.gov/show/NCT01914120

Link

https://clinicaltrials.gov/show/NCT01914120

Trefwoorden

  1. 17-01-19 17-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

17 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Non-small Cell Lung Cancer. NCT01914120

Eligibility Non-small Cell Lung Cancer. NCT01914120

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
age: >18 and <75 years old
Beschrijving

ID.1

Datatype

boolean

pathological or cytological diagnosis confirmed advanced non-small cell lung cancer
Beschrijving

ID.2

Datatype

boolean

eastern cooperative oncology group performance status: 0-2
Beschrijving

ID.3

Datatype

boolean

have never receive any kind of anti-cancer chemotherapy
Beschrijving

ID.4

Datatype

boolean

agree to regularly assessment of quality of life
Beschrijving

ID.5

Datatype

boolean

sign the informed consent form
Beschrijving

ID.6

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
currently attending any antitumor drug clinical trials
Beschrijving

ID.7

Datatype

boolean

pregnancy or breast-feeding women
Beschrijving

ID.8

Datatype

boolean

currently receiving anti-tumor chemotherapy, or received any antitumor chemotherapy previously.
Beschrijving

ID.9

Datatype

boolean

not suitable to participate in this test
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Non-small Cell Lung Cancer. NCT01914120

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
age: >18 and <75 years old
boolean
ID.2
Item
pathological or cytological diagnosis confirmed advanced non-small cell lung cancer
boolean
ID.3
Item
eastern cooperative oncology group performance status: 0-2
boolean
ID.4
Item
have never receive any kind of anti-cancer chemotherapy
boolean
ID.5
Item
agree to regularly assessment of quality of life
boolean
ID.6
Item
sign the informed consent form
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
currently attending any antitumor drug clinical trials
boolean
ID.8
Item
pregnancy or breast-feeding women
boolean
ID.9
Item
currently receiving anti-tumor chemotherapy, or received any antitumor chemotherapy previously.
boolean
ID.10
Item
not suitable to participate in this test
boolean

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