English

Eligibility Lung Cancer NCT00193453

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
to be included in the study, you must meet the following criteria:
Description

Criteria Fulfill

Data type

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
18 years of age or older
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
non-small cell lung cancer confirmed by biopsy
Description

Non-Small Cell Lung Carcinoma Biopsy

Data type

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C0005558
unresectable stage iii or iv disease
Description

Disease unresectable TNM clinical staging

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C1519810
UMLS CUI [1,3]
C3258246
measurable disease
Description

Measurable Disease

Data type

boolean

Alias
UMLS CUI [1]
C1513041
must not have received any prior chemotherapy for lung cancer
Description

Carcinoma of lung Chemotherapy Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0684249
UMLS CUI [1,2]
C0392920
UMLS CUI [1,3]
C0332197
able to perform activities of daily living without considerable assistance
Description

Activities of Daily Living Perform Able

Data type

boolean

Alias
UMLS CUI [1,1]
C0001288
UMLS CUI [1,2]
C0884358
UMLS CUI [1,3]
C0085732
adequate bone marrow, kidney, and liver function
Description

Bone Marrow function | Renal function | Liver function

Data type

boolean

Alias
UMLS CUI [1,1]
C0005953
UMLS CUI [1,2]
C0031843
UMLS CUI [2]
C0232804
UMLS CUI [3]
C0232741
signed informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
you cannot participate in the study if any of the following apply to you:
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
history of serious heart disease within six months prior to study entry
Description

Heart Disease Serious

Data type

boolean

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C0205404
prior treatment with agents that target the egfr pathway
Description

Pharmaceutical Preparations Targeting EGFR pathway

Data type

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C1521840
UMLS CUI [1,3]
C1155379
history of any other uncontrolled or significant disease
Description

Disease Uncontrolled | Disease Significant

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0205318
UMLS CUI [2,1]
C0012634
UMLS CUI [2,2]
C0750502
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have. you can then decide if you wish to participate.
Description

Clinical Trial Eligibility Criteria Additional

Data type

boolean

Alias
UMLS CUI [1,1]
C1516637
UMLS CUI [1,2]
C1524062
Back to the top of the page

Similar models

Eligibility Lung Cancer NCT00193453

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Criteria Fulfill
Item
to be included in the study, you must meet the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Age
Item
18 years of age or older
boolean
C0001779 (UMLS CUI [1])
Non-Small Cell Lung Carcinoma Biopsy
Item
non-small cell lung cancer confirmed by biopsy
boolean
C0007131 (UMLS CUI [1,1])
C0005558 (UMLS CUI [1,2])
Disease unresectable TNM clinical staging
Item
unresectable stage iii or iv disease
boolean
C0012634 (UMLS CUI [1,1])
C1519810 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
Measurable Disease
Item
measurable disease
boolean
C1513041 (UMLS CUI [1])
Carcinoma of lung Chemotherapy Absent
Item
must not have received any prior chemotherapy for lung cancer
boolean
C0684249 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Activities of Daily Living Perform Able
Item
able to perform activities of daily living without considerable assistance
boolean
C0001288 (UMLS CUI [1,1])
C0884358 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
Bone Marrow function | Renal function | Liver function
Item
adequate bone marrow, kidney, and liver function
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0232804 (UMLS CUI [2])
C0232741 (UMLS CUI [3])
Informed Consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Study Subject Participation Status
Item
you cannot participate in the study if any of the following apply to you:
boolean
C2348568 (UMLS CUI [1])
Heart Disease Serious
Item
history of serious heart disease within six months prior to study entry
boolean
C0018799 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
Pharmaceutical Preparations Targeting EGFR pathway
Item
prior treatment with agents that target the egfr pathway
boolean
C0013227 (UMLS CUI [1,1])
C1521840 (UMLS CUI [1,2])
C1155379 (UMLS CUI [1,3])
Disease Uncontrolled | Disease Significant
Item
history of any other uncontrolled or significant disease
boolean
C0012634 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0012634 (UMLS CUI [2,1])
C0750502 (UMLS CUI [2,2])
Clinical Trial Eligibility Criteria Additional
Item
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have. you can then decide if you wish to participate.
boolean
C1516637 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])
Back to the top of the page