ID

31200

Descripción

Concurrent Endostar, Paclitaxel/Carboplatin and Radiotherapy for Locally Advanced Non-small Cell Lung (RT0902); ODM derived from: https://clinicaltrials.gov/show/NCT01158144

Link

https://clinicaltrials.gov/show/NCT01158144

Palabras clave

Versiones (1)
  1. 27/7/18 27/7/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

27 de julio de 2018

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Non-small Cell Lung Cancer NCT01158144

Inglés

Eligibility Non-small Cell Lung Cancer NCT01158144

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically proven non-small cell lung cancer (squamous cell carcinoma, adenocarcinoma, large cell carcinoma and etc)
Descripción

Non-Small Cell Lung Carcinoma | Squamous cell carcinoma | Adenocarcinoma | Carcinoma, Large Cell

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007131
UMLS CUI [2]
C0007137
UMLS CUI [3]
C0001418
UMLS CUI [4]
C0206704
presence of measurable disease by recist
Descripción

Measurable Disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1513041
stage iiia or iiib, non-resectable
Descripción

TNM clinical staging | Tumor unresectable

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3258246
UMLS CUI [2,1]
C0027651
UMLS CUI [2,2]
C1519810
ecog performance status 0-1
Descripción

ECOG performance status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1520224
no prior chemotherapy, radiation therapy to chest, immunotherapy, or biologic therapy .patients must sign an informed consent indicating that they are aware of the .investigational nature of the study in keeping with the policy of the hospital.
Descripción

Prior Chemotherapy Absent | Radiotherapy to thorax Absent | Immunotherapy Absent | Biological treatment Absent | Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C4038705
UMLS CUI [2,2]
C0332197
UMLS CUI [3,1]
C0021083
UMLS CUI [3,2]
C0332197
UMLS CUI [4,1]
C1531518
UMLS CUI [4,2]
C0332197
UMLS CUI [5]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
carcinoid tumor, small cell carcinoma of lung
Descripción

Carcinoid Tumor | Small cell carcinoma of lung

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007095
UMLS CUI [2]
C0149925
patients with any distant metastasis
Descripción

Distant metastasis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1269798
history of another malignancy except cured basal cell carcinoma of skin and cured carcinoma in-situ of uterine cervix
Descripción

Cancer Other | Exception Basal cell carcinoma Cured | Exception Carcinoma in situ of uterine cervix Cured

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1707251
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0007117
UMLS CUI [2,3]
C1880198
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0851140
UMLS CUI [3,3]
C1880198
any other morbidity or situation with contraindication for radiotherapy (e.g. active infection, myocardial infarction preceding 6 months, symptomatic heart disease including unstable angina, congestive heart failure or uncontrolled arrhythmias, immunosuppressive treatment)
Descripción

Comorbidity Therapeutic radiology procedure Contraindicated | Condition Therapeutic radiology procedure Contraindicated | Communicable Disease | Myocardial Infarction | Heart Disease Symptomatic | Angina, Unstable | Congestive heart failure | Cardiac Arrhythmia Uncontrolled | Therapeutic immunosuppression

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C1522449
UMLS CUI [1,3]
C1444657
UMLS CUI [2,1]
C0348080
UMLS CUI [2,2]
C1522449
UMLS CUI [2,3]
C1444657
UMLS CUI [3]
C0009450
UMLS CUI [4]
C0027051
UMLS CUI [5,1]
C0018799
UMLS CUI [5,2]
C0231220
UMLS CUI [6]
C0002965
UMLS CUI [7]
C0018802
UMLS CUI [8,1]
C0003811
UMLS CUI [8,2]
C0205318
UMLS CUI [9]
C0021079
pregnant or lactating women, women who has not taken test of pregnancy (within 7 days before the first administration) and pregnant women
Descripción

Pregnancy | Breast Feeding | Gender Pregnancy Test Lacking

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C0079399
UMLS CUI [3,2]
C0032976
UMLS CUI [3,3]
C0332268
women and men of childbearing potential who have no willing of employing adequate contraception tumor egfr wild
Descripción

Females & males of reproductive potential Contraceptive methods Unwilling

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C4034483
UMLS CUI [1,2]
C0700589
UMLS CUI [1,3]
C0558080
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Similar models

Eligibility Non-small Cell Lung Cancer NCT01158144

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Non-Small Cell Lung Carcinoma | Squamous cell carcinoma | Adenocarcinoma | Carcinoma, Large Cell
Item
histologically proven non-small cell lung cancer (squamous cell carcinoma, adenocarcinoma, large cell carcinoma and etc)
boolean
C0007131 (UMLS CUI [1])
C0007137 (UMLS CUI [2])
C0001418 (UMLS CUI [3])
C0206704 (UMLS CUI [4])
Measurable Disease
Item
presence of measurable disease by recist
boolean
C1513041 (UMLS CUI [1])
TNM clinical staging | Tumor unresectable
Item
stage iiia or iiib, non-resectable
boolean
C3258246 (UMLS CUI [1])
C0027651 (UMLS CUI [2,1])
C1519810 (UMLS CUI [2,2])
ECOG performance status
Item
ecog performance status 0-1
boolean
C1520224 (UMLS CUI [1])
Prior Chemotherapy Absent | Radiotherapy to thorax Absent | Immunotherapy Absent | Biological treatment Absent | Informed Consent
Item
no prior chemotherapy, radiation therapy to chest, immunotherapy, or biologic therapy .patients must sign an informed consent indicating that they are aware of the .investigational nature of the study in keeping with the policy of the hospital.
boolean
C1514457 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C4038705 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0021083 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C1531518 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
C0021430 (UMLS CUI [5])
Item Group
C0680251 (UMLS CUI)
Carcinoid Tumor | Small cell carcinoma of lung
Item
carcinoid tumor, small cell carcinoma of lung
boolean
C0007095 (UMLS CUI [1])
C0149925 (UMLS CUI [2])
Distant metastasis
Item
patients with any distant metastasis
boolean
C1269798 (UMLS CUI [1])
Cancer Other | Exception Basal cell carcinoma Cured | Exception Carcinoma in situ of uterine cervix Cured
Item
history of another malignancy except cured basal cell carcinoma of skin and cured carcinoma in-situ of uterine cervix
boolean
C1707251 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0007117 (UMLS CUI [2,2])
C1880198 (UMLS CUI [2,3])
C1705847 (UMLS CUI [3,1])
C0851140 (UMLS CUI [3,2])
C1880198 (UMLS CUI [3,3])
Comorbidity Therapeutic radiology procedure Contraindicated | Condition Therapeutic radiology procedure Contraindicated | Communicable Disease | Myocardial Infarction | Heart Disease Symptomatic | Angina, Unstable | Congestive heart failure | Cardiac Arrhythmia Uncontrolled | Therapeutic immunosuppression
Item
any other morbidity or situation with contraindication for radiotherapy (e.g. active infection, myocardial infarction preceding 6 months, symptomatic heart disease including unstable angina, congestive heart failure or uncontrolled arrhythmias, immunosuppressive treatment)
boolean
C0009488 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
C1444657 (UMLS CUI [1,3])
C0348080 (UMLS CUI [2,1])
C1522449 (UMLS CUI [2,2])
C1444657 (UMLS CUI [2,3])
C0009450 (UMLS CUI [3])
C0027051 (UMLS CUI [4])
C0018799 (UMLS CUI [5,1])
C0231220 (UMLS CUI [5,2])
C0002965 (UMLS CUI [6])
C0018802 (UMLS CUI [7])
C0003811 (UMLS CUI [8,1])
C0205318 (UMLS CUI [8,2])
C0021079 (UMLS CUI [9])
Pregnancy | Breast Feeding | Gender Pregnancy Test Lacking
Item
pregnant or lactating women, women who has not taken test of pregnancy (within 7 days before the first administration) and pregnant women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0079399 (UMLS CUI [3,1])
C0032976 (UMLS CUI [3,2])
C0332268 (UMLS CUI [3,3])
Females & males of reproductive potential Contraceptive methods Unwilling
Item
women and men of childbearing potential who have no willing of employing adequate contraception tumor egfr wild
boolean
C4034483 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
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