Eligibility Lung Cancer NCT01261598

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically confirmed non-small cell lung cancer
Description

Non-Small Cell Lung Carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C0007131
fertile patients must use effective contraception
Description

Fertility Contraceptive methods

Data type

boolean

Alias
UMLS CUI [1,1]
C0015895
UMLS CUI [1,2]
C0700589
who performance status <2
Description

WHO performance status scale

Data type

boolean

Alias
UMLS CUI [1]
C1298650
measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension (≥ 10 mm with spiral ct scan)
Description

Measurable Disease | Lesion Linear Quantity | Lesion Multidimensional Quantity | Lesion size Spiral CT

Data type

boolean

Alias
UMLS CUI [1]
C1513041
UMLS CUI [2,1]
C0221198
UMLS CUI [2,2]
C0205132
UMLS CUI [2,3]
C1265611
UMLS CUI [3,1]
C0221198
UMLS CUI [3,2]
C2347299
UMLS CUI [3,3]
C1265611
UMLS CUI [4,1]
C0449453
UMLS CUI [4,2]
C0860888
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating females
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
baseline fludeoxyglucose f 18 (fdg)-positron emission tomography (pet) scan without any target lesion
Description

FDG-PET Without Target Lesion

Data type

boolean

Alias
UMLS CUI [1,1]
C3641247
UMLS CUI [1,2]
C0332288
UMLS CUI [1,3]
C2986546
unable to under pet ct evaluation
Description

PET-CT Evaluation Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C1699633
UMLS CUI [1,2]
C1261322
UMLS CUI [1,3]
C1299582
other concurrent investigational agents
Description

Investigational New Drugs

Data type

boolean

Alias
UMLS CUI [1]
C0013230
no planning to undergo curative intent radiotherapy
Description

Therapeutic radiology procedure Curative intent Planned

Data type

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C1276305
UMLS CUI [1,3]
C1301732
familial, social, geographic, or psychological conditions that would preclude study participation
Description

Condition Familial Study Subject Participation Status Excluded | Social Conditions Study Subject Participation Status Excluded | Geographic Factors Study Subject Participation Status Excluded | Mental condition Study Subject Participation Status Excluded

Data type

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0241888
UMLS CUI [1,3]
C2348568
UMLS CUI [1,4]
C0332196
UMLS CUI [2,1]
C0037403
UMLS CUI [2,2]
C2348568
UMLS CUI [2,3]
C0332196
UMLS CUI [3,1]
C0017444
UMLS CUI [3,2]
C2348568
UMLS CUI [3,3]
C0332196
UMLS CUI [4,1]
C3840291
UMLS CUI [4,2]
C2348568
UMLS CUI [4,3]
C0332196
prior malignancy progressive disease
Description

Malignant Neoplasm Progressive Disease

Data type

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C1335499

Similar models

Eligibility Lung Cancer NCT01261598

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Non-Small Cell Lung Carcinoma
Item
histologically confirmed non-small cell lung cancer
boolean
C0007131 (UMLS CUI [1])
Fertility Contraceptive methods
Item
fertile patients must use effective contraception
boolean
C0015895 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
WHO performance status scale
Item
who performance status <2
boolean
C1298650 (UMLS CUI [1])
Measurable Disease | Lesion Linear Quantity | Lesion Multidimensional Quantity | Lesion size Spiral CT
Item
measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension (≥ 10 mm with spiral ct scan)
boolean
C1513041 (UMLS CUI [1])
C0221198 (UMLS CUI [2,1])
C0205132 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C0221198 (UMLS CUI [3,1])
C2347299 (UMLS CUI [3,2])
C1265611 (UMLS CUI [3,3])
C0449453 (UMLS CUI [4,1])
C0860888 (UMLS CUI [4,2])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Breast Feeding
Item
pregnant or lactating females
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
FDG-PET Without Target Lesion
Item
baseline fludeoxyglucose f 18 (fdg)-positron emission tomography (pet) scan without any target lesion
boolean
C3641247 (UMLS CUI [1,1])
C0332288 (UMLS CUI [1,2])
C2986546 (UMLS CUI [1,3])
PET-CT Evaluation Unable
Item
unable to under pet ct evaluation
boolean
C1699633 (UMLS CUI [1,1])
C1261322 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Investigational New Drugs
Item
other concurrent investigational agents
boolean
C0013230 (UMLS CUI [1])
Therapeutic radiology procedure Curative intent Planned
Item
no planning to undergo curative intent radiotherapy
boolean
C1522449 (UMLS CUI [1,1])
C1276305 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
Condition Familial Study Subject Participation Status Excluded | Social Conditions Study Subject Participation Status Excluded | Geographic Factors Study Subject Participation Status Excluded | Mental condition Study Subject Participation Status Excluded
Item
familial, social, geographic, or psychological conditions that would preclude study participation
boolean
C0348080 (UMLS CUI [1,1])
C0241888 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
C0332196 (UMLS CUI [1,4])
C0037403 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C0332196 (UMLS CUI [2,3])
C0017444 (UMLS CUI [3,1])
C2348568 (UMLS CUI [3,2])
C0332196 (UMLS CUI [3,3])
C3840291 (UMLS CUI [4,1])
C2348568 (UMLS CUI [4,2])
C0332196 (UMLS CUI [4,3])
Malignant Neoplasm Progressive Disease
Item
prior malignancy progressive disease
boolean
C0006826 (UMLS CUI [1,1])
C1335499 (UMLS CUI [1,2])