0 Ratings
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])
    Back to the top of the page 

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