ID

22503

Beschrijving

Investigating the Biological Effects of the Addition of Zoledronic Acid to Pre-operative Chemotherapy in Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00525759

Link

https://clinicaltrials.gov/show/NCT00525759

Trefwoorden

  1. 06-06-17 06-06-17 -
Geüploaded op

6 juni 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00525759

Eligibility Breast Cancer NCT00525759

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
women with histological diagnosis of invasive breast cancer requiring neoadjuvant chemotherapy
Beschrijving

ID.1

Datatype

boolean

Alias
UMLS CUI [1,1]
C0853879
UMLS CUI [1,2]
C4272610
t2 tumour or above
Beschrijving

ID.2

Datatype

boolean

Alias
UMLS CUI [1]
C0178759
who performance status of 0,1 or 2
Beschrijving

ID.3

Datatype

boolean

Alias
UMLS CUI [1]
C1298650
must consent to or have undergone a core biopsy for diagnosis of breast cancer and consent to undergo an additional core biopsy prior to the second cycle of chemotherapy (day 5 +/- day 21)
Beschrijving

ID.4

Datatype

boolean

Alias
UMLS CUI [1]
C1318309
written informed consent
Beschrijving

ID.5

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous chemotherapy or radiotherapy to treated breast
Beschrijving

ID.6

Datatype

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C0279134
evidence of metastatic disease or recurrent breast cancer or previous malignancy (some exceptions)
Beschrijving

ID.7

Datatype

boolean

Alias
UMLS CUI [1]
C0027627
calculated creatinine clearance < 40mls/min
Beschrijving

ID.8

Datatype

boolean

Alias
UMLS CUI [1]
C0373595
prior treatment with bisphosphonates in last year or known contraindications to bisphosphonate therapy
Beschrijving

ID.9

Datatype

boolean

Alias
UMLS CUI [1]
C1563145
concurrent tamoxifen or aromatase inhibitor medication
Beschrijving

ID.10

Datatype

boolean

Alias
UMLS CUI [1,1]
C0039286
UMLS CUI [1,2]
C0593802
pregnant or lactating women
Beschrijving

ID.11

Datatype

boolean

Alias
UMLS CUI [1,1]
C0549206
UMLS CUI [1,2]
C2828358
cardiac dysfunction that precludes use of anthracycline chemotherapy
Beschrijving

ID.12

Datatype

boolean

Alias
UMLS CUI [1]
C3277906
unwilling to have extra interim biopsy
Beschrijving

ID.13

Datatype

boolean

Alias
UMLS CUI [1,1]
C0558080
UMLS CUI [1,2]
C0005560

Similar models

Eligibility Breast Cancer NCT00525759

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
women with histological diagnosis of invasive breast cancer requiring neoadjuvant chemotherapy
boolean
C0853879 (UMLS CUI [1,1])
C4272610 (UMLS CUI [1,2])
ID.2
Item
t2 tumour or above
boolean
C0178759 (UMLS CUI [1])
ID.3
Item
who performance status of 0,1 or 2
boolean
C1298650 (UMLS CUI [1])
ID.4
Item
must consent to or have undergone a core biopsy for diagnosis of breast cancer and consent to undergo an additional core biopsy prior to the second cycle of chemotherapy (day 5 +/- day 21)
boolean
C1318309 (UMLS CUI [1])
ID.5
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.6
Item
previous chemotherapy or radiotherapy to treated breast
boolean
C1514457 (UMLS CUI [1,1])
C0279134 (UMLS CUI [1,2])
ID.7
Item
evidence of metastatic disease or recurrent breast cancer or previous malignancy (some exceptions)
boolean
C0027627 (UMLS CUI [1])
ID.8
Item
calculated creatinine clearance < 40mls/min
boolean
C0373595 (UMLS CUI [1])
ID.9
Item
prior treatment with bisphosphonates in last year or known contraindications to bisphosphonate therapy
boolean
C1563145 (UMLS CUI [1])
ID.10
Item
concurrent tamoxifen or aromatase inhibitor medication
boolean
C0039286 (UMLS CUI [1,1])
C0593802 (UMLS CUI [1,2])
ID.11
Item
pregnant or lactating women
boolean
C0549206 (UMLS CUI [1,1])
C2828358 (UMLS CUI [1,2])
ID.12
Item
cardiac dysfunction that precludes use of anthracycline chemotherapy
boolean
C3277906 (UMLS CUI [1])
ID.13
Item
unwilling to have extra interim biopsy
boolean
C0558080 (UMLS CUI [1,1])
C0005560 (UMLS CUI [1,2])

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