Eligibility Breast Cancer NCT00919880

Inclusion Criteria
Beskrivning

Inclusion Criteria

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

ID.1

Datatyp

boolean

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

ID.2

Datatyp

boolean

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

ID.3

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating females
Beskrivning

ID.4

Datatyp

boolean

previous treatment for breast cancer
Beskrivning

ID.5

Datatyp

boolean

other tumor history
Beskrivning

ID.6

Datatyp

boolean

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

ID.7

Datatyp

boolean

allergy history to similar drugs
Beskrivning

ID.8

Datatyp

boolean

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

ID.9

Datatyp

boolean

resist to participate in the study
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Breast Cancer NCT00919880

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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