Eligibility Carcinoma, Non-small-cell Lung NCT00040638

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologic or cytologic diagnosis of non-small cell lung carcinoma
Descripción

ID.1

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007131
progressed while on or after treatment on platinum-based regimen
Descripción

ID.2

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0242656
UMLS CUI [1,2]
C0392920
UMLS CUI [1,3]
C0008838
patients may not have had more than one prior cytotoxic chemotherapy regimen
Descripción

ID.3

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1514457
stage iv or iiib
Descripción

ID.4

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0441772
UMLS CUI [1,2]
C0456599
age at least 18 years
Descripción

ID.5

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
adequate liver and kidney function
Descripción

ID.6

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0232741
UMLS CUI [1,2]
C0232804
adequate bone marrow function
Descripción

ID.7

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1254358
UMLS CUI [1,2]
C0005953
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy or lactation
Descripción

ID.8

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
unstable medical conditions
Descripción

ID.9

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1142435
chemotherapy, hormonal therapy, radiotherapy, radiopharmaceuticals or immunotherapy within 3 weeks of tlk286
Descripción

ID.10

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C0279025
UMLS CUI [3]
C1522449
UMLS CUI [4,1]
C0021083
UMLS CUI [4,2]
C1258106
cns metastasis unless controlled by treatment
Descripción

ID.11

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0686377

Similar models

Eligibility Carcinoma, Non-small-cell Lung NCT00040638

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
histologic or cytologic diagnosis of non-small cell lung carcinoma
boolean
C0007131 (UMLS CUI [1])
ID.2
Item
progressed while on or after treatment on platinum-based regimen
boolean
C0242656 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C0008838 (UMLS CUI [1,3])
ID.3
Item
patients may not have had more than one prior cytotoxic chemotherapy regimen
boolean
C1514457 (UMLS CUI [1])
ID.4
Item
stage iv or iiib
boolean
C0441772 (UMLS CUI [1,1])
C0456599 (UMLS CUI [1,2])
ID.5
Item
age at least 18 years
boolean
C0001779 (UMLS CUI [1])
ID.6
Item
adequate liver and kidney function
boolean
C0232741 (UMLS CUI [1,1])
C0232804 (UMLS CUI [1,2])
ID.7
Item
adequate bone marrow function
boolean
C1254358 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
ID.8
Item
pregnancy or lactation
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
ID.9
Item
unstable medical conditions
boolean
C1142435 (UMLS CUI [1])
ID.10
Item
chemotherapy, hormonal therapy, radiotherapy, radiopharmaceuticals or immunotherapy within 3 weeks of tlk286
boolean
C0392920 (UMLS CUI [1])
C0279025 (UMLS CUI [2])
C1522449 (UMLS CUI [3])
C0021083 (UMLS CUI [4,1])
C1258106 (UMLS CUI [4,2])
ID.11
Item
cns metastasis unless controlled by treatment
boolean
C0686377 (UMLS CUI [1])