ID

34154

Beschrijving

Study of Biomarkers Associated With Fatigue in Patients With Early-Stage Breast Cancer Treated With Metformin or Placebo on NCIC-CTG-MA.32; ODM derived from: https://clinicaltrials.gov/show/NCT01286233

Link

https://clinicaltrials.gov/show/NCT01286233

Trefwoorden

  1. 14-01-19 14-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

14 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01286233

Eligibility Breast Cancer NCT01286233

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
the patient must have consented to participate and must have signed and dated an appropriate irb-approved consent form that conforms to federal and institutional guidelines for the ma.32.f study before being enrolled.
Beschrijving

ID.1

Datatype

boolean

the patient must be female.
Beschrijving

ID.2

Datatype

boolean

the patient must reside in the united states or canada.
Beschrijving

ID.3

Datatype

boolean

the patient must be english-speaking.
Beschrijving

ID.4

Datatype

boolean

the patient must be eligible for randomization in the ma.32 treatment trial. (participation in the ma.32 qol study is permitted but not required.)
Beschrijving

ID.5

Datatype

boolean

the patient must not have started taking ma.32 study therapy.
Beschrijving

ID.6

Datatype

boolean

the patient must have completed primary breast radiation therapy at least two weeks prior to enrollment in ma.32.f.
Beschrijving

ID.7

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
ma.32 study therapy has been initiated.
Beschrijving

ID.8

Datatype

boolean

currently receiving radiation therapy or additional radiation therapy is planned for initiation after starting ma.32 study therapy.
Beschrijving

ID.9

Datatype

boolean

Similar models

Eligibility Breast Cancer NCT01286233

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
the patient must have consented to participate and must have signed and dated an appropriate irb-approved consent form that conforms to federal and institutional guidelines for the ma.32.f study before being enrolled.
boolean
ID.2
Item
the patient must be female.
boolean
ID.3
Item
the patient must reside in the united states or canada.
boolean
ID.4
Item
the patient must be english-speaking.
boolean
ID.5
Item
the patient must be eligible for randomization in the ma.32 treatment trial. (participation in the ma.32 qol study is permitted but not required.)
boolean
ID.6
Item
the patient must not have started taking ma.32 study therapy.
boolean
ID.7
Item
the patient must have completed primary breast radiation therapy at least two weeks prior to enrollment in ma.32.f.
boolean
Item Group
C0680251 (UMLS CUI)
ID.8
Item
ma.32 study therapy has been initiated.
boolean
ID.9
Item
currently receiving radiation therapy or additional radiation therapy is planned for initiation after starting ma.32 study therapy.
boolean

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