ID

16483

Beschrijving

A Trial Of Gemcitabine Plus Paclitaxel And Gemcitabine Plus Docetaxel In Metastatic Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00191672

Link

https://clinicaltrials.gov/show/NCT00191672

Trefwoorden

  1. 18-07-16 18-07-16 -
Geüploaded op

18 juli 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Breast Neoplasms NCT00191672

Eligibility Breast Neoplasms NCT00191672

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
advanced or metastatic breast cancer
Beschrijving

Advanced breast cancer | Carcinoma breast stage IV

Datatype

boolean

Alias
UMLS CUI [1]
C3495917
UMLS CUI [2]
C0278488
disease that can be measured by the physician or radiologic test.
Beschrijving

Measurable Disease Physician | Measurable Disease Radiology test

Datatype

boolean

Alias
UMLS CUI [1,1]
C1513041
UMLS CUI [1,2]
C0031831
UMLS CUI [2,1]
C1513041
UMLS CUI [2,2]
C0807679
may have had one chemotherapy treatment for advanced or metastatic disease.
Beschrijving

Chemotherapy advanced disease | Chemotherapy Metastatic Neoplasm

Datatype

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0679246
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C2939420
patients may have received any prior adjuvant chemotherapy, including taxane containing regimens, provided this treatment was completed at least 6 months prior to enrollment.
Beschrijving

prior adjuvant chemotherapy | taxane

Datatype

boolean

Alias
UMLS CUI [1]
C0281265
UMLS CUI [2]
C0215136
patients may have received prior hormone therapy or immunotherapy.
Beschrijving

Prior Hormone Therapy | Prior Immunotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C1514460
UMLS CUI [2]
C1514461
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with only non-measurable disease
Beschrijving

Measurable Disease

Datatype

boolean

Alias
UMLS CUI [1]
C1513041
cancer that has spread to the brain
Beschrijving

Metastatic malignant neoplasm to brain

Datatype

boolean

Alias
UMLS CUI [1]
C0220650
a patient who received a taxane with metastatic disease.
Beschrijving

taxane | Metastatic Neoplasm

Datatype

boolean

Alias
UMLS CUI [1]
C0215136
UMLS CUI [2]
C2939420
pregnancy
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
patients who received prior gemcitabine
Beschrijving

gemcitabine

Datatype

boolean

Alias
UMLS CUI [1]
C0045093

Similar models

Eligibility Breast Neoplasms NCT00191672

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Advanced breast cancer | Carcinoma breast stage IV
Item
advanced or metastatic breast cancer
boolean
C3495917 (UMLS CUI [1])
C0278488 (UMLS CUI [2])
Measurable Disease Physician | Measurable Disease Radiology test
Item
disease that can be measured by the physician or radiologic test.
boolean
C1513041 (UMLS CUI [1,1])
C0031831 (UMLS CUI [1,2])
C1513041 (UMLS CUI [2,1])
C0807679 (UMLS CUI [2,2])
Chemotherapy advanced disease | Chemotherapy Metastatic Neoplasm
Item
may have had one chemotherapy treatment for advanced or metastatic disease.
boolean
C0392920 (UMLS CUI [1,1])
C0679246 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C2939420 (UMLS CUI [2,2])
prior adjuvant chemotherapy | taxane
Item
patients may have received any prior adjuvant chemotherapy, including taxane containing regimens, provided this treatment was completed at least 6 months prior to enrollment.
boolean
C0281265 (UMLS CUI [1])
C0215136 (UMLS CUI [2])
Prior Hormone Therapy | Prior Immunotherapy
Item
patients may have received prior hormone therapy or immunotherapy.
boolean
C1514460 (UMLS CUI [1])
C1514461 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Measurable Disease
Item
patients with only non-measurable disease
boolean
C1513041 (UMLS CUI [1])
Metastatic malignant neoplasm to brain
Item
cancer that has spread to the brain
boolean
C0220650 (UMLS CUI [1])
taxane | Metastatic Neoplasm
Item
a patient who received a taxane with metastatic disease.
boolean
C0215136 (UMLS CUI [1])
C2939420 (UMLS CUI [2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
gemcitabine
Item
patients who received prior gemcitabine
boolean
C0045093 (UMLS CUI [1])

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