ID

43826

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT00445562

Nyckelord

  1. 2016-05-05 2016-05-05 -
  2. 2016-06-18 2016-06-18 -
  3. 2021-09-20 2021-09-20 -
Uppladdad den

20 september 2021

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00445562

Eligibility Breast Cancer NCT00445562

Criteria
Beskrivning

Criteria

meets 1 of the following criteria:
Beskrivning

ID.1

Datatyp

boolean

pathologically confirmed invasive breast cancer (patient)
Beskrivning

diagnosis of invasive breast cancer

Datatyp

boolean

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

ductal carcinoma in situ

Datatyp

boolean

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

sibling

Datatyp

boolean

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

sibling with breast cancer

Datatyp

boolean

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

female sibling

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0037047
UMLS CUI [1,2]
C0086287
no deceased siblings
Beskrivning

deceased siblings

Datatyp

boolean

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

full-blood related sibling

Datatyp

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
Beskrivning

receiving ecog-e1y97 or ecog-e3y92

Datatyp

boolean

Alias
UMLS CUI [1]
C1520224
patient characteristics:
Beskrivning

ID.10

Datatyp

boolean

not specified
Beskrivning

ID.11

Datatyp

boolean

prior concurrent therapy:
Beskrivning

ID.12

Datatyp

boolean

not specified
Beskrivning

ID.13

Datatyp

boolean

Similar models

Eligibility Breast Cancer NCT00445562

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
ID.1
Item
meets 1 of the following criteria:
boolean
diagnosis of invasive breast cancer
Item
pathologically confirmed invasive breast cancer (patient)
boolean
C0678222 (UMLS CUI [1])
ductal carcinoma in situ
Item
no ductal carcinoma in situ
boolean
C1527349 (UMLS CUI [1])
sibling
Item
affected or unaffected sibling
boolean
C0037047 (UMLS CUI [1])
sibling with breast cancer
Item
affected sibling must have had (or currently has) breast cancer only
boolean
C0037047 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
female sibling
Item
unaffected sibling must be female
boolean
C0037047 (UMLS CUI [1,1])
C0086287 (UMLS CUI [1,2])
deceased siblings
Item
no deceased siblings
boolean
C0037047 (UMLS CUI [1,1])
C0011065 (UMLS CUI [1,2])
full-blood related sibling
Item
must be a full-blood related sibling
boolean
C0037047 (UMLS CUI [1,1])
C1266852 (UMLS CUI [1,2])
receiving ecog-e1y97 or ecog-e3y92
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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