ID

14866

Description

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

Link

https://clinicaltrials.gov/show/NCT00153907

Keywords

  1. 5/2/16 5/2/16 -
  2. 6/26/16 6/26/16 -
Uploaded on

May 2, 2016

DOI

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License

Creative Commons BY-NC 3.0

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Eligibility Breast Cancer NCT00153907

Eligibility Breast Cancer NCT00153907

Inclusion Criteria
Description

Inclusion Criteria

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

ID.1

Data type

boolean

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

ID.2

Data type

boolean

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

ID.3

Data type

boolean

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

ID.4

Data type

boolean

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

ID.5

Data type

boolean

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

ID.6

Data type

boolean

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

ID.7

Data type

boolean

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

ID.8

Data type

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
Description

ID.9

Data type

boolean

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

ID.10

Data type

boolean

Alias
UMLS CUI [1]
C0500456
measurable disease
Description

ID.11

Data type

boolean

Alias
UMLS CUI [1]
C0012634
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior vinca alkaloids
Description

ID.12

Data type

boolean

active gastrointestinal disease or disorder
Description

ID.13

Data type

boolean

Alias
UMLS CUI [1]
C0017178
pregnant or lactating
Description

ID.14

Data type

boolean

Alias
UMLS CUI [1]
C0032961
serious co-morbid medical or psychological condition
Description

ID.15

Data type

boolean

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

ID.16

Data type

boolean

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

ID.17

Data type

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)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
histologically confirmed breast cancer with evidence of locally advanced or metastatic disease
boolean
C0678222 (UMLS CUI [1,1])
C0027627 (UMLS CUI [1,2])
ID.2
Item
female patients age 18 or older
boolean
C0079399 (UMLS CUI [1,1])
C0001779 (UMLS CUI [1,2])
ID.3
Item
no more than three prior chemotherapeutic regimens in the metastatic setting
boolean
C0392920 (UMLS CUI [1])
ID.4
Item
anc > 1,500/mm3
boolean
C0948762 (UMLS CUI [1])
ID.5
Item
platelet count > 100,000/mm3
boolean
C0005821 (UMLS CUI [1])
ID.6
Item
sgot < 3 x uln
boolean
C0201899 (UMLS CUI [1])
ID.7
Item
bilirubin < 1.5 x uln
boolean
C1278039 (UMLS CUI [1])
ID.8
Item
performance status of 0 or 1
boolean
C1520224 (UMLS CUI [1])
ID.9
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])
ID.10
Item
able to swallow and retain oral medications
boolean
C0500456 (UMLS CUI [1])
ID.11
Item
measurable disease
boolean
C0012634 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.12
Item
prior vinca alkaloids
boolean
ID.13
Item
active gastrointestinal disease or disorder
boolean
C0017178 (UMLS CUI [1])
ID.14
Item
pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
ID.15
Item
serious co-morbid medical or psychological condition
boolean
C0009488 (UMLS CUI [1])
ID.16
Item
prior bone marrow or stem cell transplant
boolean
C1504389 (UMLS CUI [1])
ID.17
Item
prior documented severe sensitivity to 5-fu
boolean
C0020517 (UMLS CUI [1,1])
C0016360 (UMLS CUI [1,2])

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