ID

14898

Description

IRESSA™ (Gefitinib) in Breast Cancer Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00632723

Link

https://clinicaltrials.gov/show/NCT00632723

Keywords

  1. 5/5/16 5/5/16 -
  2. 6/18/16 6/18/16 -
  3. 9/20/21 9/20/21 -
Uploaded on

May 5, 2016

DOI

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License

Creative Commons BY-NC 3.0

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Eligibility Breast Cancer NCT00632723

Eligibility Breast Cancer NCT00632723

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
histological or cytological confirmation of breast cancer that is either
Description

ID.1

Data type

boolean

Alias
UMLS CUI [1]
C0019638
a primary tumour in a patient unfit for or who has declined surgery
Description

ID.2

Data type

boolean

Alias
UMLS CUI [1,1]
C0677930
UMLS CUI [1,2]
C0677930|C0749186
advanced (locally or metastatic) disease
Description

ID.3

Data type

boolean

Alias
UMLS CUI [1]
C0679246
acquired resistance to tamoxifen or er negative tumour
Description

ID.4

Data type

boolean

Alias
UMLS CUI [1,1]
C0332325
UMLS CUI [1,2]
C0039286|C2584629
at least one measurable or assessable lesion
Description

ID.5

Data type

boolean

Alias
UMLS CUI [1]
C1513041
who performance status 0 - 2
Description

ID.6

Data type

boolean

Alias
UMLS CUI [1]
C1520224
life expectancy of 12 weeks or more
Description

ID.7

Data type

boolean

Alias
UMLS CUI [1]
C0023671
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
more than one previous chemotherapy regimens for advanced disease
Description

ID.8

Data type

boolean

Alias
UMLS CUI [1,1]
C0205156
UMLS CUI [1,2]
C0392920
prior anthracycline chemotherapy (> 250 mg/m2 adriamycin)
Description

ID.9

Data type

boolean

Alias
UMLS CUI [1]
C0003234
radiotherapy completed within 14 days prior to day 1 of treatment
Description

ID.10

Data type

boolean

Alias
UMLS CUI [1]
C1522449
incomplete healing from prior oncologic or other major surgery
Description

ID.11

Data type

boolean

Alias
UMLS CUI [1]
C0543478
signs of neurological symptoms consistent with spinal cord compression
Description

ID.12

Data type

boolean

Alias
UMLS CUI [1,1]
C0235031
UMLS CUI [1,2]
C0037926
any evidence of clinically active interstitial lung disease (patients with chronic stable
Description

ID.13

Data type

boolean

Alias
UMLS CUI [1]
C0206062

Similar models

Eligibility Breast Cancer NCT00632723

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
histological or cytological confirmation of breast cancer that is either
boolean
C0019638 (UMLS CUI [1])
ID.2
Item
a primary tumour in a patient unfit for or who has declined surgery
boolean
C0677930 (UMLS CUI [1,1])
C0677930|C0749186 (UMLS CUI [1,2])
ID.3
Item
advanced (locally or metastatic) disease
boolean
C0679246 (UMLS CUI [1])
ID.4
Item
acquired resistance to tamoxifen or er negative tumour
boolean
C0332325 (UMLS CUI [1,1])
C0039286|C2584629 (UMLS CUI [1,2])
ID.5
Item
at least one measurable or assessable lesion
boolean
C1513041 (UMLS CUI [1])
ID.6
Item
who performance status 0 - 2
boolean
C1520224 (UMLS CUI [1])
ID.7
Item
life expectancy of 12 weeks or more
boolean
C0023671 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.8
Item
more than one previous chemotherapy regimens for advanced disease
boolean
C0205156 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
ID.9
Item
prior anthracycline chemotherapy (> 250 mg/m2 adriamycin)
boolean
C0003234 (UMLS CUI [1])
ID.10
Item
radiotherapy completed within 14 days prior to day 1 of treatment
boolean
C1522449 (UMLS CUI [1])
ID.11
Item
incomplete healing from prior oncologic or other major surgery
boolean
C0543478 (UMLS CUI [1])
ID.12
Item
signs of neurological symptoms consistent with spinal cord compression
boolean
C0235031 (UMLS CUI [1,1])
C0037926 (UMLS CUI [1,2])
ID.13
Item
any evidence of clinically active interstitial lung disease (patients with chronic stable
boolean
C0206062 (UMLS CUI [1])

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