ID

43743

Description

Changes in Breast Density and Breast Cancer Risk in Women With Breast Cancer and in Healthy Women; ODM derived from: https://clinicaltrials.gov/show/NCT00445445

Link

https://clinicaltrials.gov/show/NCT00445445

Keywords

Versions (2)
  1. 10/5/17 10/5/17 -
  2. 9/20/21 9/20/21 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

September 20, 2021

DOI

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License

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00445445

English

Eligibility Breast Cancer NCT00445445

1 forms  
Criteria
Description

Criteria

meets 1 of the following criteria:
Description

Criteria Fulfill

Data type

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
patient at the university hospitals breast center and primary care clinics within the university hospitals system and meets the following criteria:
Description

Patient University Hospital | Criteria Fulfill

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0020028
UMLS CUI [2,1]
C0243161
UMLS CUI [2,2]
C1550543
histologically confirmed breast cancer that was diagnosed between the years 2002-2004
Description

Breast Carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C0678222
known tumor stage
Description

Tumor stage Known

Data type

boolean

Alias
UMLS CUI [1,1]
C1300072
UMLS CUI [1,2]
C0205309
healthy participant who is receiving routine medical care (e.g., screening mammograms) at the university hospitals health system
Description

Healthy participant | Routine Medical care | Screening mammography

Data type

boolean

Alias
UMLS CUI [1]
C1708335
UMLS CUI [2,1]
C0205547
UMLS CUI [2,2]
C0496675
UMLS CUI [3]
C0203028
underwent ≥ 4 prior screening mammograms at the breast center since 1994
Description

Screening mammography Quantity

Data type

boolean

Alias
UMLS CUI [1,1]
C0203028
UMLS CUI [1,2]
C1265611
no known carriers of brca1 or brca2 genes
Description

BRCA1 Mutation Carrier Excluded | BRCA2 Mutation Carrier Excluded

Data type

boolean

Alias
UMLS CUI [1,1]
C3899965
UMLS CUI [1,2]
C2828389
UMLS CUI [2,1]
C3899964
UMLS CUI [2,2]
C2828389
hormone receptor status:
Description

Hormone Receptor Status

Data type

boolean

Alias
UMLS CUI [1,1]
C0019929
UMLS CUI [1,2]
C0449438
known estrogen and/or progesterone receptor status
Description

Estrogen Receptor Status Known | Progesterone Receptor Status Known

Data type

boolean

Alias
UMLS CUI [1,1]
C0034804
UMLS CUI [1,2]
C0449438
UMLS CUI [1,3]
C0205309
UMLS CUI [2,1]
C1514471
UMLS CUI [2,2]
C0205309
patient characteristics:
Description

Client Characteristics

Data type

boolean

Alias
UMLS CUI [1]
C0815172
female
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
menopausal status not specified
Description

Menopausal Status Unspecified

Data type

boolean

Alias
UMLS CUI [1,1]
C3829127
UMLS CUI [1,2]
C0205370
no breast implants
Description

Breast implant Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0178391
UMLS CUI [1,2]
C0332197
prior concurrent therapy:
Description

Therapeutic procedure

Data type

boolean

Alias
UMLS CUI [1]
C0087111
not currently taking tamoxifen citrate, raloxifene, or aromatase inhibitors
Description

Tamoxifen Citrate Absent | Raloxifene Absent | Aromatase Inhibitors Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0079589
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0244404
UMLS CUI [2,2]
C0332197
UMLS CUI [3,1]
C0593802
UMLS CUI [3,2]
C0332197
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Similar models

Eligibility Breast Cancer NCT00445445

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Criteria Fulfill
Item
meets 1 of the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Patient University Hospital | Criteria Fulfill
Item
patient at the university hospitals breast center and primary care clinics within the university hospitals system and meets the following criteria:
boolean
C0030705 (UMLS CUI [1,1])
C0020028 (UMLS CUI [1,2])
C0243161 (UMLS CUI [2,1])
C1550543 (UMLS CUI [2,2])
Breast Carcinoma
Item
histologically confirmed breast cancer that was diagnosed between the years 2002-2004
boolean
C0678222 (UMLS CUI [1])
Tumor stage Known
Item
known tumor stage
boolean
C1300072 (UMLS CUI [1,1])
C0205309 (UMLS CUI [1,2])
Healthy participant | Routine Medical care | Screening mammography
Item
healthy participant who is receiving routine medical care (e.g., screening mammograms) at the university hospitals health system
boolean
C1708335 (UMLS CUI [1])
C0205547 (UMLS CUI [2,1])
C0496675 (UMLS CUI [2,2])
C0203028 (UMLS CUI [3])
Screening mammography Quantity
Item
underwent ≥ 4 prior screening mammograms at the breast center since 1994
boolean
C0203028 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
BRCA1 Mutation Carrier Excluded | BRCA2 Mutation Carrier Excluded
Item
no known carriers of brca1 or brca2 genes
boolean
C3899965 (UMLS CUI [1,1])
C2828389 (UMLS CUI [1,2])
C3899964 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
Hormone Receptor Status
Item
hormone receptor status:
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
Estrogen Receptor Status Known | Progesterone Receptor Status Known
Item
known estrogen and/or progesterone receptor status
boolean
C0034804 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C0205309 (UMLS CUI [1,3])
C1514471 (UMLS CUI [2,1])
C0205309 (UMLS CUI [2,2])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Menopausal Status Unspecified
Item
menopausal status not specified
boolean
C3829127 (UMLS CUI [1,1])
C0205370 (UMLS CUI [1,2])
Breast implant Absent
Item
no breast implants
boolean
C0178391 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Tamoxifen Citrate Absent | Raloxifene Absent | Aromatase Inhibitors Absent
Item
not currently taking tamoxifen citrate, raloxifene, or aromatase inhibitors
boolean
C0079589 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0244404 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0593802 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
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