Eligibility Non-Small Cell Lung Cancer NCT00529100

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
some of the requirements to be in this study are:
Description

Inclusion Criteria

Data type

boolean

Alias
UMLS CUI [1]
C1512693
patient must be at least 18 years old.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
patient must have been diagnosed with non-small cell lung cancer.
Description

Non-small cell lung cancer

Data type

boolean

Alias
UMLS CUI [1]
C0007131
patient must be able to visit the doctor's office once a week.
Description

Office Visits

Data type

boolean

Alias
UMLS CUI [1]
C0028900
patient must have adequate blood, liver, lungs and kidney function within the requirements of this study.
Description

Blood, liver, lung and kidney function

Data type

boolean

Alias
UMLS CUI [1]
C0005811
UMLS CUI [2]
C0232741
UMLS CUI [3]
C0231921
UMLS CUI [4]
C0232804
female patients of child-bearing potential must test negative for pregnancy at the time of enrollment based on a serum pregnancy test. male and female patients must agree to use a reliable method of birth control during and for 3 months following the last dose of study drug.
Description

Serum pregnancy test, Contraception

Data type

boolean

Alias
UMLS CUI [1]
C0430060
UMLS CUI [2]
C0700589
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients cannot participate in this study for any of the following reasons:
Description

Exclusion Criteria

Data type

boolean

Alias
UMLS CUI [1]
C0680251
patient has previously had chemotherapy.
Description

Previous chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0392920
patient has previously had thoracic radiation therapy.
Description

previous thoracic radiation therapy

Data type

boolean

Alias
UMLS CUI [1]
C4038705
patient has received treatment within the last 30 days with a drug that has not received approval by health canada for any indication at the time of study entry.
Description

Investigational drug

Data type

boolean

Alias
UMLS CUI [1]
C0013230
female patient is pregnant or breast-feeding.
Description

Pregnancy or breast feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patient is unsuitable to participate in the study in the opinion of the investigator.
Description

Compliance behavior

Data type

boolean

Alias
UMLS CUI [1]
C1321605
patient is unable or unwilling to take folic acid, vitamin b12 supplementation, or dexamethasone.
Description

unable or unwilling to take folic acid, vitamin b12 supplementation, or dexamethasone

Data type

boolean

Alias
UMLS CUI [1]
C0556110
UMLS CUI [2]
C3661610
UMLS CUI [3]
C0011777

Similar models

Eligibility Non-Small Cell Lung Cancer NCT00529100

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Inclusion Criteria
Item
some of the requirements to be in this study are:
boolean
C1512693 (UMLS CUI [1])
Age
Item
patient must be at least 18 years old.
boolean
C0001779 (UMLS CUI [1])
Non-small cell lung cancer
Item
patient must have been diagnosed with non-small cell lung cancer.
boolean
C0007131 (UMLS CUI [1])
Office Visits
Item
patient must be able to visit the doctor's office once a week.
boolean
C0028900 (UMLS CUI [1])
Blood, liver, lung and kidney function
Item
patient must have adequate blood, liver, lungs and kidney function within the requirements of this study.
boolean
C0005811 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
C0231921 (UMLS CUI [3])
C0232804 (UMLS CUI [4])
Serum pregnancy test, Contraception
Item
female patients of child-bearing potential must test negative for pregnancy at the time of enrollment based on a serum pregnancy test. male and female patients must agree to use a reliable method of birth control during and for 3 months following the last dose of study drug.
boolean
C0430060 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Exclusion Criteria
Item
patients cannot participate in this study for any of the following reasons:
boolean
C0680251 (UMLS CUI [1])
Previous chemotherapy
Item
patient has previously had chemotherapy.
boolean
C0392920 (UMLS CUI [1])
previous thoracic radiation therapy
Item
patient has previously had thoracic radiation therapy.
boolean
C4038705 (UMLS CUI [1])
Investigational drug
Item
patient has received treatment within the last 30 days with a drug that has not received approval by health canada for any indication at the time of study entry.
boolean
C0013230 (UMLS CUI [1])
Pregnancy or breast feeding
Item
female patient is pregnant or breast-feeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Compliance behavior
Item
patient is unsuitable to participate in the study in the opinion of the investigator.
boolean
C1321605 (UMLS CUI [1])
unable or unwilling to take folic acid, vitamin b12 supplementation, or dexamethasone
Item
patient is unable or unwilling to take folic acid, vitamin b12 supplementation, or dexamethasone.
boolean
C0556110 (UMLS CUI [1])
C3661610 (UMLS CUI [2])
C0011777 (UMLS CUI [3])