ID

34150

Beschrijving

Comparison of Neo-adjuvant Weekly Paclitaxel With or Without Carboplatin in Early Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00919880

Link

https://clinicaltrials.gov/show/NCT00919880

Trefwoorden

  1. 14-01-19 14-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

14 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00919880

Eligibility Breast Cancer NCT00919880

Inclusion Criteria
Beschrijving

Inclusion Criteria

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

ID.1

Datatype

boolean

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

ID.2

Datatype

boolean

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

ID.3

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating females
Beschrijving

ID.4

Datatype

boolean

previous treatment for breast cancer
Beschrijving

ID.5

Datatype

boolean

other tumor history
Beschrijving

ID.6

Datatype

boolean

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

ID.7

Datatype

boolean

allergy history to similar drugs
Beschrijving

ID.8

Datatype

boolean

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

ID.9

Datatype

boolean

resist to participate in the study
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Breast Cancer NCT00919880

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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

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