ID

16302

Descrizione

Neo-adjuvant Gemcitabine, Epirubicin, ABI-007 (GEA) in Locally Advanced or Inflammatory Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00193206

collegamento

https://clinicaltrials.gov/show/NCT00193206

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 NCT00193206

Eligibility Breast Cancer NCT00193206

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
locally advanced/inflammatory adenocarcinoma of the breast
Descrizione

locally advanced/inflammatory adenocarcinoma of the breast

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0858252
UMLS CUI [1,2]
C0278601
UMLS CUI [1,3]
C0677984
18 years of age or older
Descrizione

age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
normal heart function
Descrizione

heart function

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0232164
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
no prior chemotherapy for breast cancer
Descrizione

prior chemotherapy for breast cancer

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C0678222
adequate bone marrow, liver and kidney function
Descrizione

bone marrow, liver and kidney function

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0232741
UMLS CUI [1,2]
C0005953
UMLS CUI [1,3]
C0232804
no evidence or history of significant cardiovascular abnormalities
Descrizione

cardiovascular abnormalities

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0243050
sentinel node or axillary dissection
Descrizione

sentinel node or axillary dissection

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C2733271
UMLS CUI [1,2]
C0193867
sign an informed consent form
Descrizione

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
pregnant or breast feeding
Descrizione

pregnant or breast feeding

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
history of heart disease with congestive heart failure
Descrizione

heart disease with congestive heart failure

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0018802
heart attack within the previous 6 months
Descrizione

Myocardial Infarction

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0027051
prior chemotherapy or hormone therapy for breast cancer
Descrizione

prior chemotherapy or hormone therapy for breast cancer

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C1514460
UMLS CUI [1,3]
C0678222
history of active uncontrolled infection
Descrizione

active uncontrolled infection

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0009450
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 NCT00193206

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])
locally advanced/inflammatory adenocarcinoma of the breast
Item
locally advanced/inflammatory adenocarcinoma of the breast
boolean
C0858252 (UMLS CUI [1,1])
C0278601 (UMLS CUI [1,2])
C0677984 (UMLS CUI [1,3])
age
Item
18 years of age or older
boolean
C0001779 (UMLS CUI [1])
heart function
Item
normal heart function
boolean
C0232164 (UMLS CUI [1])
Ability to perform activities of daily living
Item
able to perform activities of daily living with minimal assistance
boolean
C1518965 (UMLS CUI [1])
prior chemotherapy for breast cancer
Item
no prior chemotherapy for breast cancer
boolean
C1514457 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
bone marrow, liver and kidney function
Item
adequate bone marrow, liver and kidney function
boolean
C0232741 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
C0232804 (UMLS CUI [1,3])
cardiovascular abnormalities
Item
no evidence or history of significant cardiovascular abnormalities
boolean
C0243050 (UMLS CUI [1])
sentinel node or axillary dissection
Item
sentinel node or axillary dissection
boolean
C2733271 (UMLS CUI [1,1])
C0193867 (UMLS CUI [1,2])
informed consent
Item
sign an informed consent form
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])
pregnant or breast feeding
Item
pregnant or breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
heart disease with congestive heart failure
Item
history of heart disease with congestive heart failure
boolean
C0018802 (UMLS CUI [1])
Myocardial Infarction
Item
heart attack within the previous 6 months
boolean
C0027051 (UMLS CUI [1])
prior chemotherapy or hormone therapy for breast cancer
Item
prior chemotherapy or hormone therapy for breast cancer
boolean
C1514457 (UMLS CUI [1,1])
C1514460 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
active uncontrolled infection
Item
history of active uncontrolled infection
boolean
C0009450 (UMLS CUI [1])
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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