Eligibility Breast Cancer NCT00919880

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
female patients between 18 and 65 years old
Descripción

ID.1

Tipo de datos

boolean

pathological diagnosed invasive breast cancer; medium and high risk primary breast cancer according to st. gallen 2007
Descripción

ID.2

Tipo de datos

boolean

able and willing to give consent to participate in the study
Descripción

ID.3

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating females
Descripción

ID.4

Tipo de datos

boolean

previous treatment for breast cancer
Descripción

ID.5

Tipo de datos

boolean

other tumor history
Descripción

ID.6

Tipo de datos

boolean

instable complication (e.g., myocardial infarction within 6 months, arrhythmia, unstable diabetes, hypercalcemia) or uncontrolled infection
Descripción

ID.7

Tipo de datos

boolean

allergy history to similar drugs
Descripción

ID.8

Tipo de datos

boolean

concurrent disease or condition that would make the patient inappropriate for study participation
Descripción

ID.9

Tipo de datos

boolean

resist to participate in the study
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Breast Cancer NCT00919880

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
female patients between 18 and 65 years old
boolean
ID.2
Item
pathological diagnosed invasive breast cancer; medium and high risk primary breast cancer according to st. gallen 2007
boolean
ID.3
Item
able and willing to give consent to participate in the study
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
pregnant or lactating females
boolean
ID.5
Item
previous treatment for breast cancer
boolean
ID.6
Item
other tumor history
boolean
ID.7
Item
instable complication (e.g., myocardial infarction within 6 months, arrhythmia, unstable diabetes, hypercalcemia) or uncontrolled infection
boolean
ID.8
Item
allergy history to similar drugs
boolean
ID.9
Item
concurrent disease or condition that would make the patient inappropriate for study participation
boolean
ID.10
Item
resist to participate in the study
boolean