ID

14798

Beskrivning

Randomized Trial of Fulvestrant With or Without Dasatinib in Men and Postmenopausal Women Who Have Hormone Receptor-positive Advanced Breast Cancer Previously Treated With an Aromatase Inhibitor; ODM derived from: https://clinicaltrials.gov/show/NCT00754325

Länk

https://clinicaltrials.gov/show/NCT00754325

Nyckelord

  1. 2016-04-28 2016-04-28 -
Uppladdad den

28 april 2016

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Advanced Breast Cancer NCT00754325

Eligibility Advanced Breast Cancer NCT00754325

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically confirmed hormone receptor positive (hr+) [(estrogen receptor (er+) and/or progesterone receptors(pgr+)] breast cancer according to immunohistochemistry (ihc)
Beskrivning

hormone receptor positive breast cancer

Datatyp

boolean

Alias
UMLS CUI [1]
C1562029
measureable or evaluable-only disease
Beskrivning

measureable disease

Datatyp

boolean

Alias
UMLS CUI [1]
C1513041
human epidermal growth factor receptor 2+ (her2+) or her2- breast cancer
Beskrivning

epidermal growth factor receptor breast cancer

Datatyp

boolean

Alias
UMLS CUI [1]
C1960925
males and females ≥18 years of age
Beskrivning

age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
females are post menopausal or surgically sterile
Beskrivning

post menopausal or surgically sterile

Datatyp

boolean

Alias
UMLS CUI [1]
C0021359
UMLS CUI [2]
C0232970
recurrent or progressive advanced breast cancer (locally-advanced or metastatic), that has progressed: (a) during or within 12 months after completion of adjuvant aromatase inhibitor (ai) treatment or (b) during ai treatment in advanced setting (metastatic therapy)
Beskrivning

recurrent or progressive advanced breast cancer

Datatyp

boolean

Alias
UMLS CUI [1]
C0596224
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or breast feeding
Beskrivning

pregnant or breast feeding

Datatyp

boolean

Alias
UMLS CUI [1]
C0549206
UMLS CUI [2]
C0006147
>1 chemotherapy regimen for advanced disease
Beskrivning

chemotherapy regimen

Datatyp

boolean

Alias
UMLS CUI [1]
C0392920
pleural or pericardial effusion
Beskrivning

pleural or pericardial effusion

Datatyp

boolean

Alias
UMLS CUI [1]
C0032227
UMLS CUI [2]
C0031039
serious cardiac condition
Beskrivning

cardiac condition

Datatyp

boolean

Alias
UMLS CUI [1]
C0018799

Similar models

Eligibility Advanced Breast Cancer NCT00754325

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
hormone receptor positive breast cancer
Item
histologically confirmed hormone receptor positive (hr+) [(estrogen receptor (er+) and/or progesterone receptors(pgr+)] breast cancer according to immunohistochemistry (ihc)
boolean
C1562029 (UMLS CUI [1])
measureable disease
Item
measureable or evaluable-only disease
boolean
C1513041 (UMLS CUI [1])
epidermal growth factor receptor breast cancer
Item
human epidermal growth factor receptor 2+ (her2+) or her2- breast cancer
boolean
C1960925 (UMLS CUI [1])
age
Item
males and females ≥18 years of age
boolean
C0001779 (UMLS CUI [1])
post menopausal or surgically sterile
Item
females are post menopausal or surgically sterile
boolean
C0021359 (UMLS CUI [1])
C0232970 (UMLS CUI [2])
recurrent or progressive advanced breast cancer
Item
recurrent or progressive advanced breast cancer (locally-advanced or metastatic), that has progressed: (a) during or within 12 months after completion of adjuvant aromatase inhibitor (ai) treatment or (b) during ai treatment in advanced setting (metastatic therapy)
boolean
C0596224 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
pregnant or breast feeding
Item
pregnant or breast feeding
boolean
C0549206 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
chemotherapy regimen
Item
>1 chemotherapy regimen for advanced disease
boolean
C0392920 (UMLS CUI [1])
pleural or pericardial effusion
Item
pleural or pericardial effusion
boolean
C0032227 (UMLS CUI [1])
C0031039 (UMLS CUI [2])
cardiac condition
Item
serious cardiac condition
boolean
C0018799 (UMLS CUI [1])

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