ID

15841

Beskrivning

Cytoxan, Epirubicin and Capecitabine in Women With Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00146588

Länk

https://clinicaltrials.gov/show/NCT00146588

Nyckelord

  1. 2016-06-15 2016-06-15 -
Uppladdad den

15 juni 2016

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00146588

Eligibility Breast Cancer NCT00146588

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically confirmed stage i-iii breast cancer. if stage i, should be deemed of sufficiently high risk of developing recurrent disease to warrant participation.
Beskrivning

stage i-iii breast cancer

Datatyp

boolean

Alias
UMLS CUI [1]
C0678222
18 years of age or older
Beskrivning

age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
anc > 1,000/mm3
Beskrivning

anc

Datatyp

boolean

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

platelet count

Datatyp

boolean

Alias
UMLS CUI [1]
C0005821
hemoglobin > 10
Beskrivning

hemoglobin

Datatyp

boolean

Alias
UMLS CUI [1]
C0518015
creatinine < 2.0
Beskrivning

creatinine

Datatyp

boolean

Alias
UMLS CUI [1]
C0201976
sgot < 2 x uln
Beskrivning

sgot

Datatyp

boolean

Alias
UMLS CUI [1]
C0201899
bilirubin < 1.5mg/dl
Beskrivning

bilirubin

Datatyp

boolean

Alias
UMLS CUI [1]
C0201913
able to swallow and retain oral medication
Beskrivning

oral medication

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2712086
UMLS CUI [1,2]
C0175795
lvef greater than or equal to 50%
Beskrivning

lvef

Datatyp

boolean

Alias
UMLS CUI [1]
C0428772
ecog performance status of 0 or 1
Beskrivning

ecog performance status

Datatyp

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating
Beskrivning

pregnancy or lactating

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
prior malignancy within 5 years (excluding squamous or basal cell skin cancers)
Beskrivning

prior malignancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0006826
prior chemotherapy within 5 years
Beskrivning

chemotherapy

Datatyp

boolean

Alias
UMLS CUI [1]
C0392920
prior anthracycline therapy
Beskrivning

anthracycline therapy

Datatyp

boolean

Alias
UMLS CUI [1]
C0282564
serious comorbid physical or psychological condition
Beskrivning

comorbidity

Datatyp

boolean

Alias
UMLS CUI [1]
C0009488

Similar models

Eligibility Breast Cancer NCT00146588

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
stage i-iii breast cancer
Item
histologically confirmed stage i-iii breast cancer. if stage i, should be deemed of sufficiently high risk of developing recurrent disease to warrant participation.
boolean
C0678222 (UMLS CUI [1])
age
Item
18 years of age or older
boolean
C0001779 (UMLS CUI [1])
anc
Item
anc > 1,000/mm3
boolean
C0948762 (UMLS CUI [1])
platelet count
Item
platelet count > 100,000/mm3
boolean
C0005821 (UMLS CUI [1])
hemoglobin
Item
hemoglobin > 10
boolean
C0518015 (UMLS CUI [1])
creatinine
Item
creatinine < 2.0
boolean
C0201976 (UMLS CUI [1])
sgot
Item
sgot < 2 x uln
boolean
C0201899 (UMLS CUI [1])
bilirubin
Item
bilirubin < 1.5mg/dl
boolean
C0201913 (UMLS CUI [1])
oral medication
Item
able to swallow and retain oral medication
boolean
C2712086 (UMLS CUI [1,1])
C0175795 (UMLS CUI [1,2])
lvef
Item
lvef greater than or equal to 50%
boolean
C0428772 (UMLS CUI [1])
ecog performance status
Item
ecog performance status of 0 or 1
boolean
C1520224 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
pregnancy or lactating
Item
pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
prior malignancy
Item
prior malignancy within 5 years (excluding squamous or basal cell skin cancers)
boolean
C0006826 (UMLS CUI [1])
chemotherapy
Item
prior chemotherapy within 5 years
boolean
C0392920 (UMLS CUI [1])
anthracycline therapy
Item
prior anthracycline therapy
boolean
C0282564 (UMLS CUI [1])
comorbidity
Item
serious comorbid physical or psychological condition
boolean
C0009488 (UMLS CUI [1])

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