ID

15841

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT00146588

Trefwoorden

  1. 15-06-16 15-06-16 -
Geüploaded op

15 juni 2016

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Breast Cancer NCT00146588

Eligibility Breast Cancer NCT00146588

Inclusion Criteria
Beschrijving

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.
Beschrijving

stage i-iii breast cancer

Datatype

boolean

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

age

Datatype

boolean

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

anc

Datatype

boolean

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

platelet count

Datatype

boolean

Alias
UMLS CUI [1]
C0005821
hemoglobin > 10
Beschrijving

hemoglobin

Datatype

boolean

Alias
UMLS CUI [1]
C0518015
creatinine < 2.0
Beschrijving

creatinine

Datatype

boolean

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

sgot

Datatype

boolean

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

bilirubin

Datatype

boolean

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

oral medication

Datatype

boolean

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

lvef

Datatype

boolean

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

ecog performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating
Beschrijving

pregnancy or lactating

Datatype

boolean

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

prior malignancy

Datatype

boolean

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

chemotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C0392920
prior anthracycline therapy
Beschrijving

anthracycline therapy

Datatype

boolean

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

comorbidity

Datatype

boolean

Alias
UMLS CUI [1]
C0009488

Similar models

Eligibility Breast Cancer NCT00146588

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

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial