ID

28360

Description

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

Link

https://clinicaltrials.gov/show/NCT00813137

Keywords

Versions (1)
  1. 1/7/18 1/7/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

January 7, 2018

DOI

To request one please log in.

License

Creative Commons BY 4.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Colorectal Neoplasms NCT00813137

English

Eligibility Colorectal Neoplasms NCT00813137

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

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

Colorectal cancer metastatic

Data type

boolean

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

Measurable Disease

Data type

boolean

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

ECOG performance status

Data type

boolean

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

Age

Data type

boolean

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

Life Expectancy

Data type

boolean

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

Informed Consent

Data type

boolean

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

Hematologic function | Biological function

Data type

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating women
Description

Pregnancy | Breast Feeding

Data type

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
Description

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

Data type

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
Description

Involvement Neuropathy | Involvement Brain | Involvement Leptomeningeal

Data type

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.
Description

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

Data type

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
Description

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

Data type

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
Description

Comorbidity Uncontrolled | Prior radiation therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205318
UMLS CUI [2]
C0279134
Back to the top of the page

Similar models

Eligibility Colorectal Neoplasms NCT00813137

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

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