Eligibility Non Small Cell Lung Cancer NCT00160043

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
non small cell lung cancer, stage iiib or stage iv
Beskrivning

NSCLC

Datatyp

boolean

Alias
UMLS CUI [1]
C0007131
one and only 1 prior platinum-based chemotherapy
Beskrivning

Platinum-based chemotherapy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C3536920
no other uncontrolled concurrent illness
Beskrivning

other uncontrolled concurrent illness

Datatyp

boolean

Alias
UMLS CUI [1]
C0009488
use of highly effective birth control methods in males or females with reproductive potential
Beskrivning

Contraception

Datatyp

boolean

Alias
UMLS CUI [1]
C0700589
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous participation in another trial within the last 4 weeks
Beskrivning

Study Subject Participation Status

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
surgery within 10 days prior to the start of study treatment
Beskrivning

Surgery

Datatyp

boolean

Alias
UMLS CUI [1]
C0543467
brain metastases
Beskrivning

Brain metastases

Datatyp

boolean

Alias
UMLS CUI [1]
C0220650
confirmed diagnosis of infection with the human immunodeficiency virus (hiv)
Beskrivning

HIV Infection

Datatyp

boolean

Alias
UMLS CUI [1]
C0019693
current treatment with warfarin sodium (coumadin) or similar anticoagulation medication
Beskrivning

treatment with warfarin sodium (coumadin) or similar anticoagulation medication

Datatyp

boolean

Alias
UMLS CUI [1]
C0699129
breast feeding
Beskrivning

Breast feeding

Datatyp

boolean

Alias
UMLS CUI [1]
C0006147

Similar models

Eligibility Non Small Cell Lung Cancer NCT00160043

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
NSCLC
Item
non small cell lung cancer, stage iiib or stage iv
boolean
C0007131 (UMLS CUI [1])
Platinum-based chemotherapy
Item
one and only 1 prior platinum-based chemotherapy
boolean
C0392920 (UMLS CUI [1,1])
C3536920 (UMLS CUI [1,2])
other uncontrolled concurrent illness
Item
no other uncontrolled concurrent illness
boolean
C0009488 (UMLS CUI [1])
Contraception
Item
use of highly effective birth control methods in males or females with reproductive potential
boolean
C0700589 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Study Subject Participation Status
Item
previous participation in another trial within the last 4 weeks
boolean
C2348568 (UMLS CUI [1])
Surgery
Item
surgery within 10 days prior to the start of study treatment
boolean
C0543467 (UMLS CUI [1])
Brain metastases
Item
brain metastases
boolean
C0220650 (UMLS CUI [1])
HIV Infection
Item
confirmed diagnosis of infection with the human immunodeficiency virus (hiv)
boolean
C0019693 (UMLS CUI [1])
treatment with warfarin sodium (coumadin) or similar anticoagulation medication
Item
current treatment with warfarin sodium (coumadin) or similar anticoagulation medication
boolean
C0699129 (UMLS CUI [1])
Breast feeding
Item
breast feeding
boolean
C0006147 (UMLS CUI [1])