ID

34400

Beschrijving

Polymorphism Interaction to Predict Bevacizumab Efficacy; ODM derived from: https://clinicaltrials.gov/show/NCT01935102

Link

https://clinicaltrials.gov/show/NCT01935102

Trefwoorden

  1. 17-01-19 17-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

17 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Metastatic Breast Cancer NCT01935102

Eligibility Metastatic Breast Cancer NCT01935102

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis histologically confirmed of metastatic breast cancer
Beschrijving

ID.1

Datatype

boolean

age (from 18 to 90 years)
Beschrijving

ID.2

Datatype

boolean

eastern cooperative oncology group (ecog) performance status (0 or 1-2)
Beschrijving

ID.3

Datatype

boolean

hormonal-receptor status (positive or negative)
Beschrijving

ID.4

Datatype

boolean

previous adjuvant chemotherapy (none, anthracycline or anthracycline plus taxane)
Beschrijving

ID.5

Datatype

boolean

previous hormonal therapy (adjuvant or metastatic)disease-free interval from the first diagnosis of breast cancer (≤ or >12 months)
Beschrijving

ID.6

Datatype

boolean

extent of disease (≤ or >3 sites)
Beschrijving

ID.7

Datatype

boolean

location of disease (viscera or bone)
Beschrijving

ID.8

Datatype

boolean

disease evaluation (measurable or non-measurable)and bevacizumab maintenance (yes or no).
Beschrijving

ID.9

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with human epidermal growth factor receptor type 2 (her2)-positive
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Metastatic Breast Cancer NCT01935102

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
diagnosis histologically confirmed of metastatic breast cancer
boolean
ID.2
Item
age (from 18 to 90 years)
boolean
ID.3
Item
eastern cooperative oncology group (ecog) performance status (0 or 1-2)
boolean
ID.4
Item
hormonal-receptor status (positive or negative)
boolean
ID.5
Item
previous adjuvant chemotherapy (none, anthracycline or anthracycline plus taxane)
boolean
ID.6
Item
previous hormonal therapy (adjuvant or metastatic)disease-free interval from the first diagnosis of breast cancer (≤ or >12 months)
boolean
ID.7
Item
extent of disease (≤ or >3 sites)
boolean
ID.8
Item
location of disease (viscera or bone)
boolean
ID.9
Item
disease evaluation (measurable or non-measurable)and bevacizumab maintenance (yes or no).
boolean
Item Group
C0680251 (UMLS CUI)
ID.10
Item
patients with human epidermal growth factor receptor type 2 (her2)-positive
boolean

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