ID

33982

Beskrivning

High Dose Icotinib in Advanced Non-small Cell Lung Cancer With EGFR 21 Exon Mutation; ODM derived from: https://clinicaltrials.gov/show/NCT02404675

Länk

https://clinicaltrials.gov/show/NCT02404675

Nyckelord

  1. 2019-01-09 2019-01-09 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

9 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility NSCLC NCT02404675

Eligibility NSCLC NCT02404675

  1. StudyEvent: Eligibility
    1. Eligibility NSCLC NCT02404675
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically or cytologically confirmed stage iiib/iv lung cancer(exclude patients confirmed by sputum cytology)
Beskrivning

Malignant neoplasm of lung TNM clinical staging | Sputum cytology Excluded

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0242379
UMLS CUI [1,2]
C3258246
UMLS CUI [2,1]
C0551076
UMLS CUI [2,2]
C0332196
positive egfr 21 exon mutation or 19 exon deletion
Beskrivning

EGFR Exon 21 Mutation Positive | EGFR exon 19 deletion Positive

Datatyp

boolean

Alias
UMLS CUI [1,1]
C4289654
UMLS CUI [1,2]
C1514241
UMLS CUI [2,1]
C3889117
UMLS CUI [2,2]
C1514241
age 18-75 years old with performance status of 0 to 2
Beskrivning

Age | Performance status

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C1518965
with a measurable disease(longest diameters >=10mm with spiral computed tomography (ct)and >=20mm with conventional ct) according to recist criteria
Beskrivning

Measurable Disease | Longest Diameter Spiral CT | Longest Diameter CT

Datatyp

boolean

Alias
UMLS CUI [1]
C1513041
UMLS CUI [2,1]
C0552406
UMLS CUI [2,2]
C0860888
UMLS CUI [3,1]
C0552406
UMLS CUI [3,2]
C0040405
adequate hematological, biochemical and organ functions.
Beskrivning

Hematologic function | Function Biochemical | Organ function

Datatyp

boolean

Alias
UMLS CUI [1]
C0221130
UMLS CUI [2,1]
C0031843
UMLS CUI [2,2]
C0205474
UMLS CUI [3]
C0678852
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe systemic disease out of control such as unstable or uncompensated respiratory,cardiac,liver,renal diseases.
Beskrivning

Systemic disease Severe Uncontrolled | Respiration Disorders Unstable | Heart Diseases Unstable | Liver diseases Unstable | Kidney Diseases Unstable | Respiration Disorders Uncompensated | Heart Diseases Uncompensated | Liver diseases Uncompensated | Kidney Diseases Uncompensated

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0442893
UMLS CUI [1,2]
C0205082
UMLS CUI [1,3]
C0205318
UMLS CUI [2,1]
C0035204
UMLS CUI [2,2]
C0443343
UMLS CUI [3,1]
C0018799
UMLS CUI [3,2]
C0443343
UMLS CUI [4,1]
C0023895
UMLS CUI [4,2]
C0443343
UMLS CUI [5,1]
C0022658
UMLS CUI [5,2]
C0443343
UMLS CUI [6,1]
C0035204
UMLS CUI [6,2]
C0205433
UMLS CUI [7,1]
C0018799
UMLS CUI [7,2]
C0205433
UMLS CUI [8,1]
C0023895
UMLS CUI [8,2]
C0205433
UMLS CUI [9,1]
C0022658
UMLS CUI [9,2]
C0205433
evidence of interstitial lung diseases
Beskrivning

Lung Diseases, Interstitial

Datatyp

boolean

Alias
UMLS CUI [1]
C0206062
evidence of any other significant clinical disorder or laboratory finding that makes it undesirable for the subject to participate in the study
Beskrivning

Disease Study Subject Participation Status Unfavorable | Laboratory test finding Study Subject Participation Status Unfavorable

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C3640815
UMLS CUI [2,1]
C0587081
UMLS CUI [2,2]
C2348568
UMLS CUI [2,3]
C3640815

Similar models

Eligibility NSCLC NCT02404675

  1. StudyEvent: Eligibility
    1. Eligibility NSCLC NCT02404675
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Malignant neoplasm of lung TNM clinical staging | Sputum cytology Excluded
Item
histologically or cytologically confirmed stage iiib/iv lung cancer(exclude patients confirmed by sputum cytology)
boolean
C0242379 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C0551076 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
EGFR Exon 21 Mutation Positive | EGFR exon 19 deletion Positive
Item
positive egfr 21 exon mutation or 19 exon deletion
boolean
C4289654 (UMLS CUI [1,1])
C1514241 (UMLS CUI [1,2])
C3889117 (UMLS CUI [2,1])
C1514241 (UMLS CUI [2,2])
Age | Performance status
Item
age 18-75 years old with performance status of 0 to 2
boolean
C0001779 (UMLS CUI [1])
C1518965 (UMLS CUI [2])
Measurable Disease | Longest Diameter Spiral CT | Longest Diameter CT
Item
with a measurable disease(longest diameters >=10mm with spiral computed tomography (ct)and >=20mm with conventional ct) according to recist criteria
boolean
C1513041 (UMLS CUI [1])
C0552406 (UMLS CUI [2,1])
C0860888 (UMLS CUI [2,2])
C0552406 (UMLS CUI [3,1])
C0040405 (UMLS CUI [3,2])
Hematologic function | Function Biochemical | Organ function
Item
adequate hematological, biochemical and organ functions.
boolean
C0221130 (UMLS CUI [1])
C0031843 (UMLS CUI [2,1])
C0205474 (UMLS CUI [2,2])
C0678852 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Systemic disease Severe Uncontrolled | Respiration Disorders Unstable | Heart Diseases Unstable | Liver diseases Unstable | Kidney Diseases Unstable | Respiration Disorders Uncompensated | Heart Diseases Uncompensated | Liver diseases Uncompensated | Kidney Diseases Uncompensated
Item
severe systemic disease out of control such as unstable or uncompensated respiratory,cardiac,liver,renal diseases.
boolean
C0442893 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0205318 (UMLS CUI [1,3])
C0035204 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
C0018799 (UMLS CUI [3,1])
C0443343 (UMLS CUI [3,2])
C0023895 (UMLS CUI [4,1])
C0443343 (UMLS CUI [4,2])
C0022658 (UMLS CUI [5,1])
C0443343 (UMLS CUI [5,2])
C0035204 (UMLS CUI [6,1])
C0205433 (UMLS CUI [6,2])
C0018799 (UMLS CUI [7,1])
C0205433 (UMLS CUI [7,2])
C0023895 (UMLS CUI [8,1])
C0205433 (UMLS CUI [8,2])
C0022658 (UMLS CUI [9,1])
C0205433 (UMLS CUI [9,2])
Lung Diseases, Interstitial
Item
evidence of interstitial lung diseases
boolean
C0206062 (UMLS CUI [1])
Disease Study Subject Participation Status Unfavorable | Laboratory test finding Study Subject Participation Status Unfavorable
Item
evidence of any other significant clinical disorder or laboratory finding that makes it undesirable for the subject to participate in the study
boolean
C0012634 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C3640815 (UMLS CUI [1,3])
C0587081 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C3640815 (UMLS CUI [2,3])

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