ID

34337

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT02509871

Nyckelord

  1. 2019-01-16 2019-01-16 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

16 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Hormonal Therapy NCT02509871

Eligibility Hormonal Therapy NCT02509871

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
postmenopausal women
Beskrivning

ID.1

Datatyp

boolean

patients requiring hormonal treatment
Beskrivning

ID.2

Datatyp

boolean

who performance status 0-2
Beskrivning

ID.3

Datatyp

boolean

patients initially included in metaca (au882) protocol
Beskrivning

ID.4

Datatyp

boolean

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

ID.5

Datatyp

boolean

patients who signed the informed consent form
Beskrivning

ID.6

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

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

ID.7

Datatyp

boolean

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

ID.8

Datatyp

boolean

patients carrying an electronic medical device (eg pacemaker)
Beskrivning

ID.9

Datatyp

boolean

patients who refused to sign the consent form
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Hormonal Therapy NCT02509871

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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