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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

Lien

https://clinicaltrials.gov/show/NCT00445445

Mots-clés

  1. 05/10/2017 05/10/2017 -
  2. 20/09/2021 20/09/2021 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

20 septembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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    Eligibility Breast Cancer NCT00445445

    Eligibility Breast Cancer NCT00445445

    Criteria
    Description

    Criteria

    meets 1 of the following criteria:
    Description

    Criteria Fulfill

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0243161 (criteria)
    UMLS CUI [1,2]
    C1550543 (Fulfill)
    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

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0030705 (Patients)
    SNOMED
    116154003
    UMLS CUI [1,2]
    C0020028 (Hospitals, University)
    UMLS CUI [2,1]
    C0243161 (criteria)
    UMLS CUI [2,2]
    C1550543 (Fulfill)
    histologically confirmed breast cancer that was diagnosed between the years 2002-2004
    Description

    Breast Carcinoma

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0678222 (Breast Carcinoma)
    SNOMED
    254838004
    known tumor stage
    Description

    Tumor stage Known

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C1300072 (Tumor stage)
    SNOMED
    371508000
    UMLS CUI [1,2]
    C0205309 (Known)
    SNOMED
    36692007
    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

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1708335 (Healthy Volunteers)
    UMLS CUI [2,1]
    C0205547 (Routine)
    SNOMED
    50811001
    LOINC
    LA9035-2
    UMLS CUI [2,2]
    C0496675 (Medical care)
    SNOMED
    781087000
    UMLS CUI [3]
    C0203028 (Screening mammography)
    SNOMED
    24623002
    underwent ≥ 4 prior screening mammograms at the breast center since 1994
    Description

    Screening mammography Quantity

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0203028 (Screening mammography)
    SNOMED
    24623002
    UMLS CUI [1,2]
    C1265611 (Quantity)
    SNOMED
    246205007
    LOINC
    LP202968-6
    no known carriers of brca1 or brca2 genes
    Description

    BRCA1 Mutation Carrier Excluded | BRCA2 Mutation Carrier Excluded

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C3899965 (BRCA1 Mutation Carrier)
    UMLS CUI [1,2]
    C2828389 (Exclusion)
    UMLS CUI [2,1]
    C3899964 (BRCA2 Mutation Carrier)
    UMLS CUI [2,2]
    C2828389 (Exclusion)
    hormone receptor status:
    Description

    Hormone Receptor Status

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0019929 (Hormone Receptor)
    UMLS CUI [1,2]
    C0449438 (Status)
    SNOMED
    263490005
    LOINC
    LP73412-6
    known estrogen and/or progesterone receptor status
    Description

    Estrogen Receptor Status Known | Progesterone Receptor Status Known

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0034804 (Estrogen Receptors)
    SNOMED
    23307004
    UMLS CUI [1,2]
    C0449438 (Status)
    SNOMED
    263490005
    LOINC
    LP73412-6
    UMLS CUI [1,3]
    C0205309 (Known)
    SNOMED
    36692007
    UMLS CUI [2,1]
    C1514471 (Progesterone Receptor Status)
    UMLS CUI [2,2]
    C0205309 (Known)
    SNOMED
    36692007
    patient characteristics:
    Description

    Client Characteristics

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0815172 (Client Characteristics)
    female
    Description

    Gender

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0079399 (Gender)
    SNOMED
    263495000
    LOINC
    LP61312-2
    menopausal status not specified
    Description

    Menopausal Status Unspecified

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C3829127 (Menopause Status)
    UMLS CUI [1,2]
    C0205370 (Unspecified)
    SNOMED
    10003008
    LOINC
    LA14093-1
    no breast implants
    Description

    Breast implant Absent

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0178391 (breast implant procedure)
    SNOMED
    302343007
    UMLS CUI [1,2]
    C0332197 (Absent)
    SNOMED
    2667000
    LOINC
    LA9634-2
    prior concurrent therapy:
    Description

    Therapeutic procedure

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0087111 (Therapeutic procedure)
    SNOMED
    277132007
    LOINC
    LP21090-3
    not currently taking tamoxifen citrate, raloxifene, or aromatase inhibitors
    Description

    Tamoxifen Citrate Absent | Raloxifene Absent | Aromatase Inhibitors Absent

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0079589 (tamoxifen citrate)
    SNOMED
    41395001
    UMLS CUI [1,2]
    C0332197 (Absent)
    SNOMED
    2667000
    LOINC
    LA9634-2
    UMLS CUI [2,1]
    C0244404 (raloxifene)
    SNOMED
    419530003
    UMLS CUI [2,2]
    C0332197 (Absent)
    SNOMED
    2667000
    LOINC
    LA9634-2
    UMLS CUI [3,1]
    C0593802 (Aromatase Inhibitors)
    SNOMED
    413575009
    UMLS CUI [3,2]
    C0332197 (Absent)
    SNOMED
    2667000
    LOINC
    LA9634-2

    Similar models

    Eligibility Breast Cancer NCT00445445

    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    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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