ID

14896

Description

Blood Sample Collection and Health Information Collection From Patients With Invasive Breast Cancer and Their Brothers and Sisters; ODM derived from: https://clinicaltrials.gov/show/NCT00445562

Link

https://clinicaltrials.gov/show/NCT00445562

Keywords

Versions (3)
  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 NCT00445562

English

Eligibility Breast Cancer NCT00445562

1 forms  
Criteria
Description

Criteria

meets 1 of the following criteria:
Description

ID.1

Data type

boolean

pathologically confirmed invasive breast cancer (patient)
Description

ID.2

Data type

boolean

Alias
UMLS CUI [1]
C0678222
no ductal carcinoma in situ
Description

ID.3

Data type

boolean

Alias
UMLS CUI [1]
C1527349
affected or unaffected sibling
Description

ID.4

Data type

boolean

Alias
UMLS CUI [1]
C0037047
affected sibling must have had (or currently has) breast cancer only
Description

ID.5

Data type

boolean

Alias
UMLS CUI [1,1]
C0037047
UMLS CUI [1,2]
C0678222
unaffected sibling must be female
Description

ID.6

Data type

boolean

Alias
UMLS CUI [1,1]
C0037047
UMLS CUI [1,2]
C0015780
no deceased siblings
Description

ID.7

Data type

boolean

Alias
UMLS CUI [1,1]
C0037047
UMLS CUI [1,2]
C0011065
must be a full-blood related sibling
Description

ID.8

Data type

boolean

Alias
UMLS CUI [1,1]
C0037047
UMLS CUI [1,2]
C1266852
patients receiving treatment on clinical trial ecog-e1y97 or ecog-e3y92 are not eligible
Description

ID.9

Data type

boolean

Alias
UMLS CUI [1]
C1520224
patient characteristics:
Description

ID.10

Data type

boolean

not specified
Description

ID.11

Data type

boolean

prior concurrent therapy:
Description

ID.12

Data type

boolean

not specified
Description

ID.13

Data type

boolean

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Similar models

Eligibility Breast Cancer NCT00445562

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
ID.1
Item
meets 1 of the following criteria:
boolean
ID.2
Item
pathologically confirmed invasive breast cancer (patient)
boolean
C0678222 (UMLS CUI [1])
ID.3
Item
no ductal carcinoma in situ
boolean
C1527349 (UMLS CUI [1])
ID.4
Item
affected or unaffected sibling
boolean
C0037047 (UMLS CUI [1])
ID.5
Item
affected sibling must have had (or currently has) breast cancer only
boolean
C0037047 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
ID.6
Item
unaffected sibling must be female
boolean
C0037047 (UMLS CUI [1,1])
C0015780 (UMLS CUI [1,2])
ID.7
Item
no deceased siblings
boolean
C0037047 (UMLS CUI [1,1])
C0011065 (UMLS CUI [1,2])
ID.8
Item
must be a full-blood related sibling
boolean
C0037047 (UMLS CUI [1,1])
C1266852 (UMLS CUI [1,2])
ID.9
Item
patients receiving treatment on clinical trial ecog-e1y97 or ecog-e3y92 are not eligible
boolean
C1520224 (UMLS CUI [1])
ID.10
Item
patient characteristics:
boolean
ID.11
Item
not specified
boolean
ID.12
Item
prior concurrent therapy:
boolean
ID.13
Item
not specified
boolean
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