ID

34154

Descripción

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

Palabras clave

  1. 14/1/19 14/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

14 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01286233

Eligibility Breast Cancer NCT01286233

Inclusion Criteria
Descripción

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.
Descripción

ID.1

Tipo de datos

boolean

the patient must be female.
Descripción

ID.2

Tipo de datos

boolean

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

ID.3

Tipo de datos

boolean

the patient must be english-speaking.
Descripción

ID.4

Tipo de datos

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.)
Descripción

ID.5

Tipo de datos

boolean

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

ID.6

Tipo de datos

boolean

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

ID.7

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

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

ID.8

Tipo de datos

boolean

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

ID.9

Tipo de datos

boolean

Similar models

Eligibility Breast Cancer NCT01286233

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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