ID

34164

Descripción

Study of Cardiac MRI in Patients With Left-Sided Breast Cancer Receiving Radiation Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT02199366

Link

https://clinicaltrials.gov/show/NCT02199366

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 NCT02199366

Eligibility Breast Cancer NCT02199366

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
left-sided breast cancer stage i-iii.
Descripción

ID.1

Tipo de datos

boolean

indications for adjuvant regional nodal and breast or chest wall radiation therapy (rt).
Descripción

ID.2

Tipo de datos

boolean

women and men are allowed.
Descripción

ID.3

Tipo de datos

boolean

must be at least 18 years old at time of consent.
Descripción

ID.4

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant and/or breastfeeding women or patients of child-producing potential not willing to use contraception while on study.
Descripción

ID.5

Tipo de datos

boolean

prior history of cardiovascular disease per physician discretion.
Descripción

ID.6

Tipo de datos

boolean

stage 0 and iv breast cancer.
Descripción

ID.7

Tipo de datos

boolean

prior radiation therapy to chest.
Descripción

ID.8

Tipo de datos

boolean

concurrent trastuzumab per physician discretion.
Descripción

ID.9

Tipo de datos

boolean

contraindications to cardiac mri (e.g., contrast reaction, metal implants, etc.).
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Breast Cancer NCT02199366

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
left-sided breast cancer stage i-iii.
boolean
ID.2
Item
indications for adjuvant regional nodal and breast or chest wall radiation therapy (rt).
boolean
ID.3
Item
women and men are allowed.
boolean
ID.4
Item
must be at least 18 years old at time of consent.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
pregnant and/or breastfeeding women or patients of child-producing potential not willing to use contraception while on study.
boolean
ID.6
Item
prior history of cardiovascular disease per physician discretion.
boolean
ID.7
Item
stage 0 and iv breast cancer.
boolean
ID.8
Item
prior radiation therapy to chest.
boolean
ID.9
Item
concurrent trastuzumab per physician discretion.
boolean
ID.10
Item
contraindications to cardiac mri (e.g., contrast reaction, metal implants, etc.).
boolean

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