Information:
Fel:
ID
28360
Beskrivning
FOLFOX4 Combined With Endostar in Patients With Advanced Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00813137
Länk
https://clinicaltrials.gov/show/NCT00813137
Nyckelord
Versioner (1)
- 2018-01-07 2018-01-07 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
7 januari 2018
DOI
För en begäran logga in.
Licens
Creative Commons BY 4.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
Eligibility Colorectal Neoplasms NCT00813137
Eligibility Colorectal Neoplasms NCT00813137
- StudyEvent: Eligibility
Similar models
Eligibility Colorectal Neoplasms NCT00813137
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
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])
C3714634 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
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])
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])
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])
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])
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])
C0205318 (UMLS CUI [1,2])
C0279134 (UMLS CUI [2])