Eligibility Lung Cancer NCT00193310

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
non-small cell lung cancer
Beschrijving

non-small cell lung cancer

Datatype

boolean

Alias
UMLS CUI [1]
C0007131
neoadjuvant candidates must have potentially resectable disease
Beschrijving

neoadjuvant therapy

Datatype

boolean

Alias
UMLS CUI [1]
C0600558
UMLS CUI [2]
C0015250
adjuvant candidates must have had complete resection
Beschrijving

adjuvant therapy

Datatype

boolean

Alias
UMLS CUI [1]
C0677850
UMLS CUI [2]
C0015250
clinical stage ib, ii, or iiia non-small cell lung cancer
Beschrijving

tumor stage

Datatype

boolean

Alias
UMLS CUI [1]
C1300072
ecog performance status 0 or 1
Beschrijving

ecog

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
adequate bone marrow, liver and kidney function
Beschrijving

bone marrow, liver and kidney function

Datatype

boolean

Alias
UMLS CUI [1]
C0232741
UMLS CUI [2]
C0005953
UMLS CUI [3]
C0232804
no previous chemotherapy or radiation therapy for non-small cell lung cancer.
Beschrijving

chemotherapy, radiotherapy

Datatype

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C1522449
give written informed consent.
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
stage iiia with n2 nodes > 6 cm
Beschrijving

tumor stage

Datatype

boolean

Alias
UMLS CUI [1]
C1300072
stage iiib or iv disease
Beschrijving

tumor stage

Datatype

boolean

Alias
UMLS CUI [1]
C1300072
age <18 years
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
ecog performance status 2 or higher
Beschrijving

ecog

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
considered inoperable based on general medical condition
Beschrijving

health status, inoperable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018759
UMLS CUI [1,2]
C0205187
history of prior malignancy within five years
Beschrijving

malignancy

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
women who are pregnant or lactating
Beschrijving

pregnancy, lactation

Datatype

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
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.
Beschrijving

additional criteria

Datatype

text

Similar models

Eligibility Lung Cancer NCT00193310

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
non-small cell lung cancer
Item
non-small cell lung cancer
boolean
C0007131 (UMLS CUI [1])
neoadjuvant therapy
Item
neoadjuvant candidates must have potentially resectable disease
boolean
C0600558 (UMLS CUI [1])
C0015250 (UMLS CUI [2])
adjuvant therapy
Item
adjuvant candidates must have had complete resection
boolean
C0677850 (UMLS CUI [1])
C0015250 (UMLS CUI [2])
tumor stage
Item
clinical stage ib, ii, or iiia non-small cell lung cancer
boolean
C1300072 (UMLS CUI [1])
ecog
Item
ecog performance status 0 or 1
boolean
C1520224 (UMLS CUI [1])
bone marrow, liver and kidney function
Item
adequate bone marrow, liver and kidney function
boolean
C0232741 (UMLS CUI [1])
C0005953 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
chemotherapy, radiotherapy
Item
no previous chemotherapy or radiation therapy for non-small cell lung cancer.
boolean
C0392920 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
informed consent
Item
give written informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
tumor stage
Item
stage iiia with n2 nodes > 6 cm
boolean
C1300072 (UMLS CUI [1])
tumor stage
Item
stage iiib or iv disease
boolean
C1300072 (UMLS CUI [1])
age
Item
age <18 years
boolean
C0001779 (UMLS CUI [1])
ecog
Item
ecog performance status 2 or higher
boolean
C1520224 (UMLS CUI [1])
health status, inoperable
Item
considered inoperable based on general medical condition
boolean
C0018759 (UMLS CUI [1,1])
C0205187 (UMLS CUI [1,2])
malignancy
Item
history of prior malignancy within five years
boolean
C0006826 (UMLS CUI [1])
pregnancy, lactation
Item
women who are pregnant or lactating
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
additional criteria
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.
text