ID

18533

Descripción

Trial to Evaluate Radiotherapy With or Without CBDCA in Elderly Patients With Non-Small Cell Lung Cancer (JCOG0301); ODM derived from: https://clinicaltrials.gov/show/NCT00132665

Link

https://clinicaltrials.gov/show/NCT00132665

Palabras clave

Versiones (1)
  1. 9/11/16 9/11/16 -
Subido en

9 de noviembre de 2016

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Non-Small-Cell Lung Carcinoma NCT00132665

Inglés

Eligibility Non-Small-Cell Lung Carcinoma NCT00132665

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically and/or cytologically proven nsclc
Descripción

Non-Small Cell Lung Carcinoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007131
unresectable disease
Descripción

Disease unresectable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C1519810
stage iiia except t3n1m0 and iiib which does not have disease extended to any contralateral hilar nodes, atelectasis of the entire lung or malignant pleural effusions
Descripción

TNM clinical staging | Extent of disease Hilar node Contralateral | Atelectasis Entire lung | Pleural Effusion, Malignant

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3258246
UMLS CUI [2,1]
C0449279
UMLS CUI [2,2]
C1305372
UMLS CUI [2,3]
C0441988
UMLS CUI [3,1]
C0004144
UMLS CUI [3,2]
C1278908
UMLS CUI [4]
C0080032
a required radiation field of less than one half of one lung
Descripción

Radiation Field Less Than Half Lung

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1882536
UMLS CUI [1,2]
C0439092
UMLS CUI [1,3]
C2825407
UMLS CUI [1,4]
C0024109
measurable disease
Descripción

Measurable Disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1513041
no previous chemotherapy or radiotherapy
Descripción

Prior Chemotherapy | prior radiation therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1514457
UMLS CUI [2]
C0279134
age >= 71
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
unable to receive cisplatin-based combination chemotherapy
Descripción

Combination Chemotherapy Cisplatin Based | Combination Chemotherapy Receive Unable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1521750
UMLS CUI [1,2]
C0008838
UMLS CUI [1,3]
C1705938
UMLS CUI [2,1]
C1521750
UMLS CUI [2,2]
C1514756
UMLS CUI [2,3]
C1299582
ecog performance status (ps) of 0-2
Descripción

ECOG performance status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1520224
adequate bone marrow, lung, hepatic, and renal function
Descripción

Bone Marrow function | Pulmonary function | Liver function | Renal function

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0005953
UMLS CUI [1,2]
C0031843
UMLS CUI [2]
C0231921
UMLS CUI [3]
C0232741
UMLS CUI [4]
C0232804
written informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
active infection, diarrhea, ileus, uncontrolled diabetes, myocardial infarction within three months, or severe other comorbidity
Descripción

Communicable Disease | Diarrhea | Ileus | Diabetic - poor control | Myocardial Infarction | Comorbidity Severe

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0011991
UMLS CUI [3]
C1258215
UMLS CUI [4]
C0421258
UMLS CUI [5]
C0027051
UMLS CUI [6,1]
C0009488
UMLS CUI [6,2]
C0205082
synchronous cancer or metachronous (within 5 years) malignancy
Descripción

Neoplasms, Multiple Primary | Metachronous Malignant Neoplasm

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027663
UMLS CUI [2]
C1334703
interstitial pneumonia or active lung fibrosis on chest x-ray
Descripción

Pneumonia, Interstitial | Pulmonary Fibrosis | Plain chest X-ray

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0206061
UMLS CUI [2]
C0034069
UMLS CUI [3]
C0039985
severe chronic obstructive pulmonary disease, chronic bronchitis, or bronchial asthma
Descripción

Severe chronic obstructive pulmonary disease | Bronchitis, Chronic | Asthma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0730607
UMLS CUI [2]
C0008677
UMLS CUI [3]
C0004096
pleural or pericardial effusion
Descripción

Pleural effusion | Pericardial effusion

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032227
UMLS CUI [2]
C0031039
a history of severe hypersensitivity
Descripción

severe allergy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2945656
mental disorder
Descripción

Mental disorder

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004936
judging of inappropriate condition for this study by physician
Descripción

Condition Inappropriate Clinical Trial

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C1548788
UMLS CUI [1,3]
C0008976
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Similar models

Eligibility Non-Small-Cell Lung Carcinoma NCT00132665

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Non-Small Cell Lung Carcinoma
Item
histologically and/or cytologically proven nsclc
boolean
C0007131 (UMLS CUI [1])
Disease unresectable
Item
unresectable disease
boolean
C0012634 (UMLS CUI [1,1])
C1519810 (UMLS CUI [1,2])
TNM clinical staging | Extent of disease Hilar node Contralateral | Atelectasis Entire lung | Pleural Effusion, Malignant
Item
stage iiia except t3n1m0 and iiib which does not have disease extended to any contralateral hilar nodes, atelectasis of the entire lung or malignant pleural effusions
boolean
C3258246 (UMLS CUI [1])
C0449279 (UMLS CUI [2,1])
C1305372 (UMLS CUI [2,2])
C0441988 (UMLS CUI [2,3])
C0004144 (UMLS CUI [3,1])
C1278908 (UMLS CUI [3,2])
C0080032 (UMLS CUI [4])
Radiation Field Less Than Half Lung
Item
a required radiation field of less than one half of one lung
boolean
C1882536 (UMLS CUI [1,1])
C0439092 (UMLS CUI [1,2])
C2825407 (UMLS CUI [1,3])
C0024109 (UMLS CUI [1,4])
Measurable Disease
Item
measurable disease
boolean
C1513041 (UMLS CUI [1])
Prior Chemotherapy | prior radiation therapy
Item
no previous chemotherapy or radiotherapy
boolean
C1514457 (UMLS CUI [1])
C0279134 (UMLS CUI [2])
Age
Item
age >= 71
boolean
C0001779 (UMLS CUI [1])
Combination Chemotherapy Cisplatin Based | Combination Chemotherapy Receive Unable
Item
unable to receive cisplatin-based combination chemotherapy
boolean
C1521750 (UMLS CUI [1,1])
C0008838 (UMLS CUI [1,2])
C1705938 (UMLS CUI [1,3])
C1521750 (UMLS CUI [2,1])
C1514756 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
ECOG performance status
Item
ecog performance status (ps) of 0-2
boolean
C1520224 (UMLS CUI [1])
Bone Marrow function | Pulmonary function | Liver function | Renal function
Item
adequate bone marrow, lung, hepatic, and renal function
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0231921 (UMLS CUI [2])
C0232741 (UMLS CUI [3])
C0232804 (UMLS CUI [4])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Communicable Disease | Diarrhea | Ileus | Diabetic - poor control | Myocardial Infarction | Comorbidity Severe
Item
active infection, diarrhea, ileus, uncontrolled diabetes, myocardial infarction within three months, or severe other comorbidity
boolean
C0009450 (UMLS CUI [1])
C0011991 (UMLS CUI [2])
C1258215 (UMLS CUI [3])
C0421258 (UMLS CUI [4])
C0027051 (UMLS CUI [5])
C0009488 (UMLS CUI [6,1])
C0205082 (UMLS CUI [6,2])
Neoplasms, Multiple Primary | Metachronous Malignant Neoplasm
Item
synchronous cancer or metachronous (within 5 years) malignancy
boolean
C0027663 (UMLS CUI [1])
C1334703 (UMLS CUI [2])
Pneumonia, Interstitial | Pulmonary Fibrosis | Plain chest X-ray
Item
interstitial pneumonia or active lung fibrosis on chest x-ray
boolean
C0206061 (UMLS CUI [1])
C0034069 (UMLS CUI [2])
C0039985 (UMLS CUI [3])
Severe chronic obstructive pulmonary disease | Bronchitis, Chronic | Asthma
Item
severe chronic obstructive pulmonary disease, chronic bronchitis, or bronchial asthma
boolean
C0730607 (UMLS CUI [1])
C0008677 (UMLS CUI [2])
C0004096 (UMLS CUI [3])
Pleural effusion | Pericardial effusion
Item
pleural or pericardial effusion
boolean
C0032227 (UMLS CUI [1])
C0031039 (UMLS CUI [2])
severe allergy
Item
a history of severe hypersensitivity
boolean
C2945656 (UMLS CUI [1])
Mental disorder
Item
mental disorder
boolean
C0004936 (UMLS CUI [1])
Condition Inappropriate Clinical Trial
Item
judging of inappropriate condition for this study by physician
boolean
C0348080 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
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