ID

34164

Description

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

Keywords

  1. 1/14/19 1/14/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 14, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT02199366

Eligibility Breast Cancer NCT02199366

Inclusion Criteria
Description

Inclusion Criteria

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

ID.1

Data type

boolean

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

ID.2

Data type

boolean

women and men are allowed.
Description

ID.3

Data type

boolean

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

ID.4

Data type

boolean

Exclusion Criteria
Description

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.
Description

ID.5

Data type

boolean

prior history of cardiovascular disease per physician discretion.
Description

ID.6

Data type

boolean

stage 0 and iv breast cancer.
Description

ID.7

Data type

boolean

prior radiation therapy to chest.
Description

ID.8

Data type

boolean

concurrent trastuzumab per physician discretion.
Description

ID.9

Data type

boolean

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

ID.10

Data type

boolean

Similar models

Eligibility Breast Cancer NCT02199366

Name
Type
Description | Question | Decode (Coded Value)
Data type
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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