ID

28360

Descripción

FOLFOX4 Combined With Endostar in Patients With Advanced Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00813137

Link

https://clinicaltrials.gov/show/NCT00813137

Palabras clave

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

See clinicaltrials.gov

Subido en

7 de enero de 2018

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Colorectal Neoplasms NCT00813137

Inglés

Eligibility Colorectal Neoplasms NCT00813137

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with histologically or cytologically confirmed metastatic crc
Descripción

Colorectal cancer metastatic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0948380
measurable disease according to response criteria in solid tumours (recist)
Descripción

Measurable Disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1513041
performance status 0 - 2 according to ecog (eastern cooperative oncology group) performance status
Descripción

ECOG performance status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1520224
age 18~75
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
life expectancy > 3 months
Descripción

Life Expectancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023671
signed informed consent (ic)
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
adequate haematological and biological functions
Descripción

Hematologic function | Biological function

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0221130
UMLS CUI [2]
C3714634
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating women
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to the study drugs
Descripción

Drug Allergy Relationship Investigational New Drugs | Drug Allergy Delayed Relationship Investigational New Drugs | Idiosyncrasy Pharmaceutical Preparations Relationship Investigational New Drugs

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013182
UMLS CUI [1,2]
C0439849
UMLS CUI [1,3]
C0013230
UMLS CUI [2,1]
C0013182
UMLS CUI [2,2]
C0205421
UMLS CUI [2,3]
C0439849
UMLS CUI [2,4]
C0013230
UMLS CUI [3,1]
C0231191
UMLS CUI [3,2]
C0013227
UMLS CUI [3,3]
C0439849
UMLS CUI [3,4]
C0013230
neuropathy, brain, or leptomeningeal involvement
Descripción

Involvement Neuropathy | Involvement Brain | Involvement Leptomeningeal

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1314939
UMLS CUI [1,2]
C0442874
UMLS CUI [2,1]
C1314939
UMLS CUI [2,2]
C0006104
UMLS CUI [3,1]
C1314939
UMLS CUI [3,2]
C0521401
treatment with any biologic, cytotoxic, radiation , or hormonal therapy within four weeks.
Descripción

Biological treatment | Cytotoxic therapy | Therapeutic radiology procedure | Hormone Therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1531518
UMLS CUI [2]
C0677881
UMLS CUI [3]
C1522449
UMLS CUI [4]
C0279025
clinically relevant coronary artery disease or a history of a myocardial infarction within the last 12 months or high risk/uncontrolled arrhythmia
Descripción

Coronary Artery Disease | Myocardial Infarction | Cardiac Arrhythmia High risk of | Cardiac Arrhythmia Uncontrolled

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1956346
UMLS CUI [2]
C0027051
UMLS CUI [3,1]
C0003811
UMLS CUI [3,2]
C0332167
UMLS CUI [4,1]
C0003811
UMLS CUI [4,2]
C0205318
uncontrolled significant comorbid conditions and previous radiotherapy
Descripción

Comorbidity Uncontrolled | Prior radiation therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205318
UMLS CUI [2]
C0279134
Volver a la parte superior de la página

Similar models

Eligibility Colorectal Neoplasms NCT00813137

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Colorectal cancer metastatic
Item
patients with histologically or cytologically confirmed metastatic crc
boolean
C0948380 (UMLS CUI [1])
Measurable Disease
Item
measurable disease according to response criteria in solid tumours (recist)
boolean
C1513041 (UMLS CUI [1])
ECOG performance status
Item
performance status 0 - 2 according to ecog (eastern cooperative oncology group) performance status
boolean
C1520224 (UMLS CUI [1])
Age
Item
age 18~75
boolean
C0001779 (UMLS CUI [1])
Life Expectancy
Item
life expectancy > 3 months
boolean
C0023671 (UMLS CUI [1])
Informed Consent
Item
signed informed consent (ic)
boolean
C0021430 (UMLS CUI [1])
Hematologic function | Biological function
Item
adequate haematological and biological functions
boolean
C0221130 (UMLS CUI [1])
C3714634 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Breast Feeding
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Drug Allergy Relationship Investigational New Drugs | Drug Allergy Delayed Relationship Investigational New Drugs | Idiosyncrasy Pharmaceutical Preparations Relationship Investigational New Drugs
Item
known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to the study drugs
boolean
C0013182 (UMLS CUI [1,1])
C0439849 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,3])
C0013182 (UMLS CUI [2,1])
C0205421 (UMLS CUI [2,2])
C0439849 (UMLS CUI [2,3])
C0013230 (UMLS CUI [2,4])
C0231191 (UMLS CUI [3,1])
C0013227 (UMLS CUI [3,2])
C0439849 (UMLS CUI [3,3])
C0013230 (UMLS CUI [3,4])
Involvement Neuropathy | Involvement Brain | Involvement Leptomeningeal
Item
neuropathy, brain, or leptomeningeal involvement
boolean
C1314939 (UMLS CUI [1,1])
C0442874 (UMLS CUI [1,2])
C1314939 (UMLS CUI [2,1])
C0006104 (UMLS CUI [2,2])
C1314939 (UMLS CUI [3,1])
C0521401 (UMLS CUI [3,2])
Biological treatment | Cytotoxic therapy | Therapeutic radiology procedure | Hormone Therapy
Item
treatment with any biologic, cytotoxic, radiation , or hormonal therapy within four weeks.
boolean
C1531518 (UMLS CUI [1])
C0677881 (UMLS CUI [2])
C1522449 (UMLS CUI [3])
C0279025 (UMLS CUI [4])
Coronary Artery Disease | Myocardial Infarction | Cardiac Arrhythmia High risk of | Cardiac Arrhythmia Uncontrolled
Item
clinically relevant coronary artery disease or a history of a myocardial infarction within the last 12 months or high risk/uncontrolled arrhythmia
boolean
C1956346 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
C0003811 (UMLS CUI [3,1])
C0332167 (UMLS CUI [3,2])
C0003811 (UMLS CUI [4,1])
C0205318 (UMLS CUI [4,2])
Comorbidity Uncontrolled | Prior radiation therapy
Item
uncontrolled significant comorbid conditions and previous radiotherapy
boolean
C0009488 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0279134 (UMLS CUI [2])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial