ID

34164

Beschrijving

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

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 NCT02199366

Eligibility Breast Cancer NCT02199366

Inclusion Criteria
Beschrijving

Inclusion Criteria

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

ID.1

Datatype

boolean

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

ID.2

Datatype

boolean

women and men are allowed.
Beschrijving

ID.3

Datatype

boolean

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

ID.4

Datatype

boolean

Exclusion Criteria
Beschrijving

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.
Beschrijving

ID.5

Datatype

boolean

prior history of cardiovascular disease per physician discretion.
Beschrijving

ID.6

Datatype

boolean

stage 0 and iv breast cancer.
Beschrijving

ID.7

Datatype

boolean

prior radiation therapy to chest.
Beschrijving

ID.8

Datatype

boolean

concurrent trastuzumab per physician discretion.
Beschrijving

ID.9

Datatype

boolean

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

ID.10

Datatype

boolean

Similar models

Eligibility Breast Cancer NCT02199366

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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