ID

34166

Descrição

Feasibility Study of Stereotactic Body Radiotherapy for Early Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02065960

Link

https://clinicaltrials.gov/show/NCT02065960

Palavras-chave

  1. 14/01/2019 14/01/2019 -
Titular dos direitos

see on clinicaltrials.gov

Transferido a

14 de janeiro de 2019

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Breast Neoplasm NCT02065960

Eligibility Breast Neoplasm NCT02065960

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
women age ≥ 70 years;
Descrição

ID.1

Tipo de dados

boolean

new histological diagnosis of invasive carcinoma of the breast, grade i or ii, estrogen and progesterone receptor (er and pr) positive, her2 negative on needle biopsy and limited to stage i (t1 n0 m0) on clinical and radiological assessment with mri of the breasts and axillary ultrasound;
Descrição

ID.2

Tipo de dados

boolean

candidate for breast conserving surgery;
Descrição

ID.3

Tipo de dados

boolean

signed study consent form completed prior to study entry.
Descrição

ID.4

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
breast cancer with disease within 5 mm from skin or chest wall;
Descrição

ID.5

Tipo de dados

boolean

previous or concomitant invasive malignancies treated within 5 years of study entry;
Descrição

ID.6

Tipo de dados

boolean

serious non-malignant disease (cardiovascular, pulmonary, systemic lupus or scleroderma), which would preclude to definitive radiation therapy;
Descrição

ID.7

Tipo de dados

boolean

psychiatric disorders, which would preclude from obtaining informed consent
Descrição

ID.8

Tipo de dados

boolean

geographic inaccessibility for follow-up
Descrição

ID.9

Tipo de dados

boolean

Similar models

Eligibility Breast Neoplasm NCT02065960

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
women age ≥ 70 years;
boolean
ID.2
Item
new histological diagnosis of invasive carcinoma of the breast, grade i or ii, estrogen and progesterone receptor (er and pr) positive, her2 negative on needle biopsy and limited to stage i (t1 n0 m0) on clinical and radiological assessment with mri of the breasts and axillary ultrasound;
boolean
ID.3
Item
candidate for breast conserving surgery;
boolean
ID.4
Item
signed study consent form completed prior to study entry.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
breast cancer with disease within 5 mm from skin or chest wall;
boolean
ID.6
Item
previous or concomitant invasive malignancies treated within 5 years of study entry;
boolean
ID.7
Item
serious non-malignant disease (cardiovascular, pulmonary, systemic lupus or scleroderma), which would preclude to definitive radiation therapy;
boolean
ID.8
Item
psychiatric disorders, which would preclude from obtaining informed consent
boolean
ID.9
Item
geographic inaccessibility for follow-up
boolean

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