ID

34166

Descrizione

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

collegamento

https://clinicaltrials.gov/show/NCT02065960

Keywords

  1. 14/01/19 14/01/19 -
Titolare del copyright

see on clinicaltrials.gov

Caricato su

14 gennaio 2019

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

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Eligibility Breast Neoplasm NCT02065960

Eligibility Breast Neoplasm NCT02065960

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
women age ≥ 70 years;
Descrizione

ID.1

Tipo di dati

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;
Descrizione

ID.2

Tipo di dati

boolean

candidate for breast conserving surgery;
Descrizione

ID.3

Tipo di dati

boolean

signed study consent form completed prior to study entry.
Descrizione

ID.4

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

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

ID.5

Tipo di dati

boolean

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

ID.6

Tipo di dati

boolean

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

ID.7

Tipo di dati

boolean

psychiatric disorders, which would preclude from obtaining informed consent
Descrizione

ID.8

Tipo di dati

boolean

geographic inaccessibility for follow-up
Descrizione

ID.9

Tipo di dati

boolean

Similar models

Eligibility Breast Neoplasm NCT02065960

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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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