ID

34204

Beschrijving

RAS Switch in Patients With Metastatic RAS Native Colorectal Tumors Treated With 1st Line FOLFIRI-Cetuximab; ODM derived from: https://clinicaltrials.gov/show/NCT01943786

Link

https://clinicaltrials.gov/show/NCT01943786

Trefwoorden

  1. 15-01-19 15-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

15 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Colorectal Cancer Metastatic NCT01943786

Eligibility Colorectal Cancer Metastatic NCT01943786

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of stage iv colorectal adenocarcinoma.
Beschrijving

ID.1

Datatype

boolean

patient ≥ 18 years of age.
Beschrijving

ID.2

Datatype

boolean

ecog ps 0-1
Beschrijving

ID.3

Datatype

boolean

life expectancy ≥ 6 months
Beschrijving

ID.4

Datatype

boolean

candidate for first-line systemic chemotherapy according to regular clinical practice.
Beschrijving

ID.5

Datatype

boolean

measurable disease.
Beschrijving

ID.6

Datatype

boolean

wild-type kras
Beschrijving

ID.7

Datatype

boolean

signed informed consent form.
Beschrijving

ID.8

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient who has received prior chemotherapy for metastatic crc, except for adjuvant treatment completed at least six months before entering study.
Beschrijving

ID.9

Datatype

boolean

patient in whom there is a contraindication for the use of any of the drugs used in first-line treatment of colorectal cancer: 5-fluorouracil,, irinotecan or cetuximab
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Colorectal Cancer Metastatic NCT01943786

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
diagnosis of stage iv colorectal adenocarcinoma.
boolean
ID.2
Item
patient ≥ 18 years of age.
boolean
ID.3
Item
ecog ps 0-1
boolean
ID.4
Item
life expectancy ≥ 6 months
boolean
ID.5
Item
candidate for first-line systemic chemotherapy according to regular clinical practice.
boolean
ID.6
Item
measurable disease.
boolean
ID.7
Item
wild-type kras
boolean
ID.8
Item
signed informed consent form.
boolean
Item Group
C0680251 (UMLS CUI)
ID.9
Item
patient who has received prior chemotherapy for metastatic crc, except for adjuvant treatment completed at least six months before entering study.
boolean
ID.10
Item
patient in whom there is a contraindication for the use of any of the drugs used in first-line treatment of colorectal cancer: 5-fluorouracil,, irinotecan or cetuximab
boolean

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