ID

22104

Beschrijving

Second-Line Irinotecan or Gefitinib in Docetaxel Pretreated NSCLC; ODM derived from: https://clinicaltrials.gov/show/NCT00319800

Link

https://clinicaltrials.gov/show/NCT00319800

Trefwoorden

Versies (1)
  1. 19-05-17 19-05-17 -
Geüploaded op

19 mei 2017

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Non-Small Cell Lung Cancer NCT00319800

Engels

Eligibility Non-Small Cell Lung Cancer NCT00319800

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 75 years or less
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
histologically or cytologically confirmed non-small cell lung cancer
Beschrijving

Non-Small Cell Lung Carcinoma

Datatype

boolean

Alias
UMLS CUI [1]
C0007131
advanced, metastatic or recurrent
Beschrijving

Non-Small Cell Lung Carcinoma Advanced | Non-small cell lung cancer metastatic | Non-small cell lung cancer recurrent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C0205179
UMLS CUI [2]
C0278987
UMLS CUI [3]
C0278517
ecog performance status 0 to 2
Beschrijving

ECOG performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
one prior palliative chemotherapy including docetaxel
Beschrijving

Chemotherapy Palliative Quantity | docetaxel

Datatype

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C1285530
UMLS CUI [1,3]
C1265611
UMLS CUI [2]
C0246415
measurable or evaluable indicator lesion(s)
Beschrijving

Measurable lesion | Lesion Evaluable

Datatype

boolean

Alias
UMLS CUI [1]
C1513041
UMLS CUI [2,1]
C0221198
UMLS CUI [2,2]
C1516986
normal marrow, hepatic and renal function
Beschrijving

Bone Marrow function | Liver function | Renal function

Datatype

boolean

Alias
UMLS CUI [1,1]
C0005953
UMLS CUI [1,2]
C0031843
UMLS CUI [2]
C0232741
UMLS CUI [3]
C0232804
provision of written informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
active infection and/or severe comorbidities
Beschrijving

Communicable Diseases | Comorbidity Severe

Datatype

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2,1]
C0009488
UMLS CUI [2,2]
C0205082
pregnant or breastfed women
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
active cns metastasis
Beschrijving

CNS metastases

Datatype

boolean

Alias
UMLS CUI [1]
C0686377
active bleeding in gi tract or elsewhere
Beschrijving

Gastrointestinal Hemorrhage | Hemorrhage

Datatype

boolean

Alias
UMLS CUI [1]
C0017181
UMLS CUI [2]
C0019080
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Similar models

Eligibility Non-Small Cell Lung Cancer NCT00319800

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
aged 75 years or less
boolean
C0001779 (UMLS CUI [1])
Non-Small Cell Lung Carcinoma
Item
histologically or cytologically confirmed non-small cell lung cancer
boolean
C0007131 (UMLS CUI [1])
Non-Small Cell Lung Carcinoma Advanced | Non-small cell lung cancer metastatic | Non-small cell lung cancer recurrent
Item
advanced, metastatic or recurrent
boolean
C0007131 (UMLS CUI [1,1])
C0205179 (UMLS CUI [1,2])
C0278987 (UMLS CUI [2])
C0278517 (UMLS CUI [3])
ECOG performance status
Item
ecog performance status 0 to 2
boolean
C1520224 (UMLS CUI [1])
Chemotherapy Palliative Quantity | docetaxel
Item
one prior palliative chemotherapy including docetaxel
boolean
C0392920 (UMLS CUI [1,1])
C1285530 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0246415 (UMLS CUI [2])
Measurable lesion | Lesion Evaluable
Item
measurable or evaluable indicator lesion(s)
boolean
C1513041 (UMLS CUI [1])
C0221198 (UMLS CUI [2,1])
C1516986 (UMLS CUI [2,2])
Bone Marrow function | Liver function | Renal function
Item
normal marrow, hepatic and renal function
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
Informed Consent
Item
provision of written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Communicable Diseases | Comorbidity Severe
Item
active infection and/or severe comorbidities
boolean
C0009450 (UMLS CUI [1])
C0009488 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
pregnant or breastfed women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
CNS metastases
Item
active cns metastasis
boolean
C0686377 (UMLS CUI [1])
Gastrointestinal Hemorrhage | Hemorrhage
Item
active bleeding in gi tract or elsewhere
boolean
C0017181 (UMLS CUI [1])
C0019080 (UMLS CUI [2])
Terug naar het begin van de pagina 

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