ID

16009

Beschrijving

Navelbine and Capecitabine in the Treatment of Metastatic Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00153907

Link

https://clinicaltrials.gov/show/NCT00153907

Trefwoorden

  1. 02-05-16 02-05-16 -
  2. 26-06-16 26-06-16 -
Geüploaded op

26 juni 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00153907

Eligibility Breast Cancer NCT00153907

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically confirmed breast cancer with evidence of locally advanced or metastatic disease
Beschrijving

locally advanced breast cancer

Datatype

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0027627
female patients age 18 or older
Beschrijving

female and aged over 18

Datatype

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0001779
no more than three prior chemotherapeutic regimens in the metastatic setting
Beschrijving

prior chemotherapeutic regimens

Datatype

boolean

Alias
UMLS CUI [1]
C0392920
anc > 1,500/mm3
Beschrijving

neutrophil count

Datatype

boolean

Alias
UMLS CUI [1]
C0948762
platelet count > 100,000/mm3
Beschrijving

platelet count

Datatype

boolean

Alias
UMLS CUI [1]
C0005821
sgot < 3 x uln
Beschrijving

GOT

Datatype

boolean

Alias
UMLS CUI [1]
C0201899
bilirubin < 1.5 x uln
Beschrijving

bilirubin

Datatype

boolean

Alias
UMLS CUI [1]
C1278039
performance status of 0 or 1
Beschrijving

ECOG performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
at least 3 weeks since prior chemotherapy or 2 weeks since prior radiation, surgery or any anticancer investigational agent
Beschrijving

interval since prior anticancer treatment

Datatype

boolean

Alias
UMLS CUI [1,1]
C3541383
UMLS CUI [1,2]
C0920425
able to swallow and retain oral medications
Beschrijving

dysphagia

Datatype

boolean

Alias
UMLS CUI [1]
C0500456
measurable disease
Beschrijving

measurable disease

Datatype

boolean

Alias
UMLS CUI [1]
C1513041
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior vinca alkaloids
Beschrijving

prior therapy with vinca-alkaloids

Datatype

boolean

Alias
UMLS CUI [1,1]
C0042672
UMLS CUI [1,2]
C0392920
active gastrointestinal disease or disorder
Beschrijving

gastrointestinal disease

Datatype

boolean

Alias
UMLS CUI [1]
C0017178
pregnant or lactating
Beschrijving

pregnant or lactating

Datatype

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
serious co-morbid medical or psychological condition
Beschrijving

serious comorbidities

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
prior bone marrow or stem cell transplant
Beschrijving

prior bone marrow or stem cell transplant

Datatype

boolean

Alias
UMLS CUI [1]
C1504389
prior documented severe sensitivity to 5-fu
Beschrijving

hypersensitivity to fluorouracil

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0016360

Similar models

Eligibility Breast Cancer NCT00153907

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
locally advanced breast cancer
Item
histologically confirmed breast cancer with evidence of locally advanced or metastatic disease
boolean
C0678222 (UMLS CUI [1,1])
C0027627 (UMLS CUI [1,2])
female and aged over 18
Item
female patients age 18 or older
boolean
C0079399 (UMLS CUI [1,1])
C0001779 (UMLS CUI [1,2])
prior chemotherapeutic regimens
Item
no more than three prior chemotherapeutic regimens in the metastatic setting
boolean
C0392920 (UMLS CUI [1])
neutrophil count
Item
anc > 1,500/mm3
boolean
C0948762 (UMLS CUI [1])
platelet count
Item
platelet count > 100,000/mm3
boolean
C0005821 (UMLS CUI [1])
GOT
Item
sgot < 3 x uln
boolean
C0201899 (UMLS CUI [1])
bilirubin
Item
bilirubin < 1.5 x uln
boolean
C1278039 (UMLS CUI [1])
ECOG performance status
Item
performance status of 0 or 1
boolean
C1520224 (UMLS CUI [1])
interval since prior anticancer treatment
Item
at least 3 weeks since prior chemotherapy or 2 weeks since prior radiation, surgery or any anticancer investigational agent
boolean
C3541383 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
dysphagia
Item
able to swallow and retain oral medications
boolean
C0500456 (UMLS CUI [1])
measurable disease
Item
measurable disease
boolean
C1513041 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
prior therapy with vinca-alkaloids
Item
prior vinca alkaloids
boolean
C0042672 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
gastrointestinal disease
Item
active gastrointestinal disease or disorder
boolean
C0017178 (UMLS CUI [1])
pregnant or lactating
Item
pregnant or lactating
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
serious comorbidities
Item
serious co-morbid medical or psychological condition
boolean
C0009488 (UMLS CUI [1])
prior bone marrow or stem cell transplant
Item
prior bone marrow or stem cell transplant
boolean
C1504389 (UMLS CUI [1])
hypersensitivity to fluorouracil
Item
prior documented severe sensitivity to 5-fu
boolean
C0020517 (UMLS CUI [1,1])
C0016360 (UMLS CUI [1,2])

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