ID

34337

Beschrijving

Study of Body Composition in Patients Treated by Adjuvant Hormonal Therapy for Breast Cancer (MetaCa2); ODM derived from: https://clinicaltrials.gov/show/NCT02509871

Link

https://clinicaltrials.gov/show/NCT02509871

Trefwoorden

  1. 16/01/2019 16/01/2019 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

16 de janeiro de 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Hormonal Therapy NCT02509871

Eligibility Hormonal Therapy NCT02509871

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
postmenopausal women
Beschrijving

ID.1

Datatype

boolean

patients requiring hormonal treatment
Beschrijving

ID.2

Datatype

boolean

who performance status 0-2
Beschrijving

ID.3

Datatype

boolean

patients initially included in metaca (au882) protocol
Beschrijving

ID.4

Datatype

boolean

affiliation to a social security scheme (or be the beneficiary of such a plan)
Beschrijving

ID.5

Datatype

boolean

patients who signed the informed consent form
Beschrijving

ID.6

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients witg relapse, with metastases or other cancer
Beschrijving

ID.7

Datatype

boolean

concurrent treatment with a drug test, or participation in a clinical trial within < 30 days
Beschrijving

ID.8

Datatype

boolean

patients carrying an electronic medical device (eg pacemaker)
Beschrijving

ID.9

Datatype

boolean

patients who refused to sign the consent form
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Hormonal Therapy NCT02509871

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
postmenopausal women
boolean
ID.2
Item
patients requiring hormonal treatment
boolean
ID.3
Item
who performance status 0-2
boolean
ID.4
Item
patients initially included in metaca (au882) protocol
boolean
ID.5
Item
affiliation to a social security scheme (or be the beneficiary of such a plan)
boolean
ID.6
Item
patients who signed the informed consent form
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
patients witg relapse, with metastases or other cancer
boolean
ID.8
Item
concurrent treatment with a drug test, or participation in a clinical trial within < 30 days
boolean
ID.9
Item
patients carrying an electronic medical device (eg pacemaker)
boolean
ID.10
Item
patients who refused to sign the consent form
boolean

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