ID

16301

Descrizione

Docetaxel Plus Imatinib Mesylate in Metastatic Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00193180

collegamento

https://clinicaltrials.gov/show/NCT00193180

Keywords

  1. 10/07/16 10/07/16 -
Caricato su

10 luglio 2016

DOI

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Licenza

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00193180

Eligibility Breast Cancer NCT00193180

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
to be included in this study, you must meet the following criteria:
Descrizione

Inclusion Criteria

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1512693
metastatic breast cancer confirmed by biopsy
Descrizione

metastatic breast cancer

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0278488
no more than one prior chemotherapy regimen for metastatic breast cancer
Descrizione

prior chemotherapy regimen for metastatic breast cancer

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C0278488
able to perform activities of daily living with minimal assistance
Descrizione

ability to perform activities of daily living

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1518965
adequate bone marrow, liver and kidney function
Descrizione

adequate bone marrow, liver and kidney function

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0005953
UMLS CUI [1,2]
C0232741
UMLS CUI [1,3]
C0232804
age 18 years or older
Descrizione

age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
give written informed consent
Descrizione

Written Informed Consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
you cannot participate in this study if any of the following apply to you:
Descrizione

Exclusion Criteria

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0680251
moderate to severe peripheral neuropathy
Descrizione

moderate to severe peripheral neuropathy

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0031117
UMLS CUI [1,2]
C0439793
uncontrolled blood pressure or uncontrolled heart beat irregularities
Descrizione

uncontrolled blood pressure or uncontrolled heart beat irregularities

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0005823
UMLS CUI [2]
C0003811
diabetes mellitus with fasting blood sugar greater than 200 mg %
Descrizione

diabetes mellitus with fasting blood sugar greater than 200 mg %

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0011849
UMLS CUI [1,2]
C2825162
significant heart disease within the prior 6 months
Descrizione

Heart disease

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0018799
severe or uncontrolled medical disease
Descrizione

severe or uncontrolled medical disease

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0009488
active uncontrolled infection
Descrizione

Infection

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0009450
known chronic liver disease
Descrizione

chronic liver disease

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0341439
known diagnosis of hiv infection
Descrizione

HIV Infection

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0019693
pregnant or breast feeding females
Descrizione

pregnant or breast feeding

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
Descrizione

Additional Criteria

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1516637

Similar models

Eligibility Breast Cancer NCT00193180

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Inclusion Criteria
Item
to be included in this study, you must meet the following criteria:
boolean
C1512693 (UMLS CUI [1])
metastatic breast cancer
Item
metastatic breast cancer confirmed by biopsy
boolean
C0278488 (UMLS CUI [1])
prior chemotherapy regimen for metastatic breast cancer
Item
no more than one prior chemotherapy regimen for metastatic breast cancer
boolean
C1514457 (UMLS CUI [1,1])
C0278488 (UMLS CUI [1,2])
ability to perform activities of daily living
Item
able to perform activities of daily living with minimal assistance
boolean
C1518965 (UMLS CUI [1])
adequate bone marrow, liver and kidney function
Item
adequate bone marrow, liver and kidney function
boolean
C0005953 (UMLS CUI [1,1])
C0232741 (UMLS CUI [1,2])
C0232804 (UMLS CUI [1,3])
age
Item
age 18 years or older
boolean
C0001779 (UMLS CUI [1])
Written Informed Consent
Item
give written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Exclusion Criteria
Item
you cannot participate in this study if any of the following apply to you:
boolean
C0680251 (UMLS CUI [1])
moderate to severe peripheral neuropathy
Item
moderate to severe peripheral neuropathy
boolean
C0031117 (UMLS CUI [1,1])
C0439793 (UMLS CUI [1,2])
uncontrolled blood pressure or uncontrolled heart beat irregularities
Item
uncontrolled blood pressure or uncontrolled heart beat irregularities
boolean
C0005823 (UMLS CUI [1])
C0003811 (UMLS CUI [2])
diabetes mellitus with fasting blood sugar greater than 200 mg %
Item
diabetes mellitus with fasting blood sugar greater than 200 mg %
boolean
C0011849 (UMLS CUI [1,1])
C2825162 (UMLS CUI [1,2])
Heart disease
Item
significant heart disease within the prior 6 months
boolean
C0018799 (UMLS CUI [1])
severe or uncontrolled medical disease
Item
severe or uncontrolled medical disease
boolean
C0009488 (UMLS CUI [1])
Infection
Item
active uncontrolled infection
boolean
C0009450 (UMLS CUI [1])
chronic liver disease
Item
known chronic liver disease
boolean
C0341439 (UMLS CUI [1])
HIV Infection
Item
known diagnosis of hiv infection
boolean
C0019693 (UMLS CUI [1])
pregnant or breast feeding
Item
pregnant or breast feeding females
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Additional Criteria
Item
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
boolean
C1516637 (UMLS CUI [1])

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