ID

34337

Description

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

Keywords

  1. 1/16/19 1/16/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 16, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Hormonal Therapy NCT02509871

Eligibility Hormonal Therapy NCT02509871

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
postmenopausal women
Description

ID.1

Data type

boolean

patients requiring hormonal treatment
Description

ID.2

Data type

boolean

who performance status 0-2
Description

ID.3

Data type

boolean

patients initially included in metaca (au882) protocol
Description

ID.4

Data type

boolean

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

ID.5

Data type

boolean

patients who signed the informed consent form
Description

ID.6

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

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

ID.7

Data type

boolean

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

ID.8

Data type

boolean

patients carrying an electronic medical device (eg pacemaker)
Description

ID.9

Data type

boolean

patients who refused to sign the consent form
Description

ID.10

Data type

boolean

Similar models

Eligibility Hormonal Therapy NCT02509871

Name
Type
Description | Question | Decode (Coded Value)
Data type
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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