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Eligibility Non-Small Cell Lung Cancer NCT00333294

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
signed informed consent.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
18 to 75 years inclusive.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
at least one measurable lesions histologically confirmed inoperable stage iii nsclc.
Description

Measurable Disease Quantity | Non-Small Cell Lung Carcinoma Inoperable | TNM clinical staging

Data type

boolean

Alias
UMLS CUI [1,1]
C1513041
UMLS CUI [1,2]
C1265611
UMLS CUI [2,1]
C0007131
UMLS CUI [2,2]
C0205187
UMLS CUI [3]
C3258246
who performance status of 0 to 2 inclusive.
Description

WHO performance status scale

Data type

boolean

Alias
UMLS CUI [1]
C1298650
adequate pulmonary function, pulmonary dose volume histogram less than or equal to 40
Description

Pulmonary function | Dose Volume Histogram Pulmonary

Data type

boolean

Alias
UMLS CUI [1]
C0231921
UMLS CUI [2,1]
C3827011
UMLS CUI [2,2]
C2709248
life expectancy of at least 6 months.
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
using secure contraceptives precautions.
Description

Contraceptive methods Effective

Data type

boolean

Alias
UMLS CUI [1,1]
C0700589
UMLS CUI [1,2]
C1280519
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
any previous anti cancer therapy for nsclc.
Description

cancer treatment Non-Small Cell Lung Carcinoma

Data type

boolean

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C0007131
known severe hypersensitivity to these products
Description

severe allergy products

Data type

boolean

Alias
UMLS CUI [1,1]
C2945656
UMLS CUI [1,2]
C1514468
any evidence of clinically active interstitial lung disease
Description

Interstitial Lung Disease Evidence of

Data type

boolean

Alias
UMLS CUI [1,1]
C0206062
UMLS CUI [1,2]
C0332120
other co-existing malignancies, symptomatic metastases.
Description

Malignant Neoplasms | Neoplasm Metastasis Symptomatic

Data type

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2,1]
C0027627
UMLS CUI [2,2]
C0231220
abnormal blood test
Description

Blood test abnormal

Data type

boolean

Alias
UMLS CUI [1]
C0854146
weight loss of over 15% in the 3 months before the start of the study.
Description

Weight decreased Percentage

Data type

boolean

Alias
UMLS CUI [1,1]
C1262477
UMLS CUI [1,2]
C0439165
treatment with a non-approved or investigational drug within 30 days before day 1 of study treatment.
Description

Drugs, Non-Prescription | Investigational New Drugs

Data type

boolean

Alias
UMLS CUI [1]
C0013231
UMLS CUI [2]
C0013230
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Similar models

Eligibility Non-Small Cell Lung Cancer NCT00333294

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
signed informed consent.
boolean
C0021430 (UMLS CUI [1])
Age
Item
18 to 75 years inclusive.
boolean
C0001779 (UMLS CUI [1])
Measurable Disease Quantity | Non-Small Cell Lung Carcinoma Inoperable | TNM clinical staging
Item
at least one measurable lesions histologically confirmed inoperable stage iii nsclc.
boolean
C1513041 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0007131 (UMLS CUI [2,1])
C0205187 (UMLS CUI [2,2])
C3258246 (UMLS CUI [3])
WHO performance status scale
Item
who performance status of 0 to 2 inclusive.
boolean
C1298650 (UMLS CUI [1])
Pulmonary function | Dose Volume Histogram Pulmonary
Item
adequate pulmonary function, pulmonary dose volume histogram less than or equal to 40
boolean
C0231921 (UMLS CUI [1])
C3827011 (UMLS CUI [2,1])
C2709248 (UMLS CUI [2,2])
Life Expectancy
Item
life expectancy of at least 6 months.
boolean
C0023671 (UMLS CUI [1])
Contraceptive methods Effective
Item
using secure contraceptives precautions.
boolean
C0700589 (UMLS CUI [1,1])
C1280519 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
cancer treatment Non-Small Cell Lung Carcinoma
Item
any previous anti cancer therapy for nsclc.
boolean
C0920425 (UMLS CUI [1,1])
C0007131 (UMLS CUI [1,2])
severe allergy products
Item
known severe hypersensitivity to these products
boolean
C2945656 (UMLS CUI [1,1])
C1514468 (UMLS CUI [1,2])
Interstitial Lung Disease Evidence of
Item
any evidence of clinically active interstitial lung disease
boolean
C0206062 (UMLS CUI [1,1])
C0332120 (UMLS CUI [1,2])
Malignant Neoplasms | Neoplasm Metastasis Symptomatic
Item
other co-existing malignancies, symptomatic metastases.
boolean
C0006826 (UMLS CUI [1])
C0027627 (UMLS CUI [2,1])
C0231220 (UMLS CUI [2,2])
Blood test abnormal
Item
abnormal blood test
boolean
C0854146 (UMLS CUI [1])
Weight decreased Percentage
Item
weight loss of over 15% in the 3 months before the start of the study.
boolean
C1262477 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
Drugs, Non-Prescription | Investigational New Drugs
Item
treatment with a non-approved or investigational drug within 30 days before day 1 of study treatment.
boolean
C0013231 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
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