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Eligibility Carcinoma, Non-Small-Cell Lung NCT00568841

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
written informed consent
Beskrivning

Informed Consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
≥ 18 years of age
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
untreated non-small-cell lung cancer stage iiib/iv
Beskrivning

Non-Small Cell Lung Carcinoma untreated TNM clinical staging

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C0332155
UMLS CUI [1,3]
C3258246
life expectancy > 3 months
Beskrivning

Life Expectancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0023671
performance status ecog 0-2
Beskrivning

ECOG performance status

Datatyp

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
concurrent systemic immune therapy, chemotherapy or therapy with any anticancer drug not indicated in the study protocol
Beskrivning

Immunotherapy Systemic | Chemotherapy | Antineoplastic Agents

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0021083
UMLS CUI [1,2]
C0205373
UMLS CUI [2]
C0392920
UMLS CUI [3]
C0003392
any investigational agent(s) within 4 weeks prior to study entry
Beskrivning

Investigational New Drugs

Datatyp

boolean

Alias
UMLS CUI [1]
C0013230
previous administration of any egfr-targeted therapy (antibodies, small molecules and others)
Beskrivning

Targeted Therapy Epidermal Growth Factor Receptor | Antibodies | Small Molecule

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2985566
UMLS CUI [1,2]
C0034802
UMLS CUI [2]
C3495458
UMLS CUI [3]
C1328819
any medical, mental or psychological condition which in the opinion of the investigator would not permit the patient to complete the study or understand the patient information
Beskrivning

Medical condition Excludes Clinical Trial Completion | Medical condition Preventing Comprehension Patient Information | Mental disorder Excludes Clinical Trial Completion | Mental disorder Preventing Comprehension Patient Information

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0332196
UMLS CUI [1,3]
C0008976
UMLS CUI [1,4]
C0205197
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C1292733
UMLS CUI [2,3]
C0162340
UMLS CUI [2,4]
C1955348
UMLS CUI [3,1]
C0004936
UMLS CUI [3,2]
C0332196
UMLS CUI [3,3]
C0008976
UMLS CUI [3,4]
C0205197
UMLS CUI [4,1]
C0004936
UMLS CUI [4,2]
C1292733
UMLS CUI [4,3]
C0162340
UMLS CUI [4,4]
C1955348
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Similar models

Eligibility Carcinoma, Non-Small-Cell Lung NCT00568841

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Age
Item
≥ 18 years of age
boolean
C0001779 (UMLS CUI [1])
Non-Small Cell Lung Carcinoma untreated TNM clinical staging
Item
untreated non-small-cell lung cancer stage iiib/iv
boolean
C0007131 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
Life Expectancy
Item
life expectancy > 3 months
boolean
C0023671 (UMLS CUI [1])
ECOG performance status
Item
performance status ecog 0-2
boolean
C1520224 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Immunotherapy Systemic | Chemotherapy | Antineoplastic Agents
Item
concurrent systemic immune therapy, chemotherapy or therapy with any anticancer drug not indicated in the study protocol
boolean
C0021083 (UMLS CUI [1,1])
C0205373 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2])
C0003392 (UMLS CUI [3])
Investigational New Drugs
Item
any investigational agent(s) within 4 weeks prior to study entry
boolean
C0013230 (UMLS CUI [1])
Targeted Therapy Epidermal Growth Factor Receptor | Antibodies | Small Molecule
Item
previous administration of any egfr-targeted therapy (antibodies, small molecules and others)
boolean
C2985566 (UMLS CUI [1,1])
C0034802 (UMLS CUI [1,2])
C3495458 (UMLS CUI [2])
C1328819 (UMLS CUI [3])
Medical condition Excludes Clinical Trial Completion | Medical condition Preventing Comprehension Patient Information | Mental disorder Excludes Clinical Trial Completion | Mental disorder Preventing Comprehension Patient Information
Item
any medical, mental or psychological condition which in the opinion of the investigator would not permit the patient to complete the study or understand the patient information
boolean
C3843040 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0205197 (UMLS CUI [1,4])
C3843040 (UMLS CUI [2,1])
C1292733 (UMLS CUI [2,2])
C0162340 (UMLS CUI [2,3])
C1955348 (UMLS CUI [2,4])
C0004936 (UMLS CUI [3,1])
C0332196 (UMLS CUI [3,2])
C0008976 (UMLS CUI [3,3])
C0205197 (UMLS CUI [3,4])
C0004936 (UMLS CUI [4,1])
C1292733 (UMLS CUI [4,2])
C0162340 (UMLS CUI [4,3])
C1955348 (UMLS CUI [4,4])
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