ID

34428

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT01914120

Nyckelord

  1. 2019-01-17 2019-01-17 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

17 januari 2019

DOI

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Licens

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
Beskrivning

Inclusion Criteria

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

ID.1

Datatyp

boolean

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

ID.2

Datatyp

boolean

eastern cooperative oncology group performance status: 0-2
Beskrivning

ID.3

Datatyp

boolean

have never receive any kind of anti-cancer chemotherapy
Beskrivning

ID.4

Datatyp

boolean

agree to regularly assessment of quality of life
Beskrivning

ID.5

Datatyp

boolean

sign the informed consent form
Beskrivning

ID.6

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

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

ID.7

Datatyp

boolean

pregnancy or breast-feeding women
Beskrivning

ID.8

Datatyp

boolean

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

ID.9

Datatyp

boolean

not suitable to participate in this test
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Non-small Cell Lung Cancer. NCT01914120

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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