ID

14626

Description

Study of Larotaxel in Combination With Weekly Herceptin® in Patients With HER2 Positive Metastatic Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00387907

Link

https://clinicaltrials.gov/show/NCT00387907

Keywords

Versions (1)
  1. 4/24/16 4/24/16 -
Uploaded on

April 24, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Advanced Breast Cancer NCT00387907

English

Eligibility Advanced Breast Cancer NCT00387907

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of breast cancer
Description

breast cancer

Data type

boolean

Alias
UMLS CUI [1]
C0678222
evidence that cancer has spread beyond its original location or has come back and cannot be removed by surgery
Description

metastases

Data type

boolean

Alias
UMLS CUI [1]
C0027627
no more than one prior treatment for advanced disease
Description

prior treatment

Data type

boolean

Alias
UMLS CUI [1]
C1514463
her2 positive status
Description

her2 positive

Data type

boolean

Alias
UMLS CUI [1]
C1960398
adequate liver and kidney function
Description

adequate liver and kidney function

Data type

boolean

Alias
UMLS CUI [1]
C0232741
UMLS CUI [2]
C0232804
no remaining severe harmful effects to prior treatments
Description

adverse effect

Data type

boolean

Alias
UMLS CUI [1]
C0879626
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
certain heart condition
Description

heart condition

Data type

boolean

Alias
UMLS CUI [1]
C3842523
pregnant women
Description

pregnant women

Data type

boolean

Alias
UMLS CUI [1]
C0032961
history of another cancer except some skin cancers and cervical cancer
Description

history of another cancer

Data type

boolean

Alias
UMLS CUI [1]
C1512706
taking other treatments for your cancer at the time you enter the trial
Description

cancer treatment

Data type

boolean

Alias
UMLS CUI [1]
C0920425
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Similar models

Eligibility Advanced Breast Cancer NCT00387907

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
breast cancer
Item
diagnosis of breast cancer
boolean
C0678222 (UMLS CUI [1])
metastases
Item
evidence that cancer has spread beyond its original location or has come back and cannot be removed by surgery
boolean
C0027627 (UMLS CUI [1])
prior treatment
Item
no more than one prior treatment for advanced disease
boolean
C1514463 (UMLS CUI [1])
her2 positive
Item
her2 positive status
boolean
C1960398 (UMLS CUI [1])
adequate liver and kidney function
Item
adequate liver and kidney function
boolean
C0232741 (UMLS CUI [1])
C0232804 (UMLS CUI [2])
adverse effect
Item
no remaining severe harmful effects to prior treatments
boolean
C0879626 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
heart condition
Item
certain heart condition
boolean
C3842523 (UMLS CUI [1])
pregnant women
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
history of another cancer
Item
history of another cancer except some skin cancers and cervical cancer
boolean
C1512706 (UMLS CUI [1])
cancer treatment
Item
taking other treatments for your cancer at the time you enter the trial
boolean
C0920425 (UMLS CUI [1])
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