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ID

42603

Beschreibung

Evaluation of Patients With Breast Cancer Using DCE-MRI, MRS, and Proteomics; ODM derived from: https://clinicaltrials.gov/show/NCT00656604

Link

https://clinicaltrials.gov/show/NCT00656604

Stichworte

Versionen (2)
  1. 15.07.16 15.07.16 -
  2. 17.09.21 17.09.21 -
Hochgeladen am

17. September 2021

DOI

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Lizenz

Creative Commons BY 4.0
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    Eligibility Breast Cancer NCT00656604

    Englisch

    Eligibility Breast Cancer NCT00656604

    1 Formulare  
    Criteria
    Beschreibung

    Criteria

    meets 1 of the following criteria:
    Beschreibung

    criteria Fulfill

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0243161
    UMLS CUI [1,2]
    C1550543
    women with breast tumors planning to undergo surgical resection
    Beschreibung

    Gender | Breast Carcinoma | Excision Planned

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0079399
    UMLS CUI [2]
    C0678222
    UMLS CUI [3,1]
    C0728940
    UMLS CUI [3,2]
    C1301732
    healthy volunteers, including any constitutionally healthy female with no history of breast cancer
    Beschreibung

    Healthy Volunteers | Well female adult | Breast Carcinoma

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C1708335
    UMLS CUI [2]
    C0686752
    UMLS CUI [3]
    C0678222
    hormone receptor status not specified
    Beschreibung

    Hormone Receptor Status Unspecified

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0019929
    UMLS CUI [1,2]
    C0449438
    UMLS CUI [1,3]
    C0205370
    patient characteristics:
    Beschreibung

    patient characteristics

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0815172
    female
    Beschreibung

    Gender

    Datentyp

    boolean

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

    Menopausal Status Unspecified

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C3829127
    UMLS CUI [1,2]
    C0205370
    not pregnant or nursing
    Beschreibung

    Pregnancy | Breast Feeding

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2]
    C0006147
    negative pregnancy test
    Beschreibung

    Pregnancy test negative

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0427780
    fertile patients must use effective contraception
    Beschreibung

    Fertility Contraceptive methods

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0015895
    UMLS CUI [1,2]
    C0700589
    not acutely ill
    Beschreibung

    Illness

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0221423
    no non-magnetic resonance-compatible ferromagnetic materials present in the body
    Beschreibung

    Foreign materials Magnetic metal Present Body

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0016542
    UMLS CUI [1,2]
    C0439876
    UMLS CUI [1,3]
    C0150312
    UMLS CUI [1,4]
    C1268086
    prior concurrent therapy:
    Beschreibung

    concurrent therapy

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0009429
    prior chemotherapy and/or radiotherapy allowed
    Beschreibung

    Prior Chemotherapy | prior radiation therapy

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C1514457
    UMLS CUI [2]
    C0279134
    Zum Seitenanfang zurückkehren

    Ähnliche Modelle

    Eligibility Breast Cancer NCT00656604

    1 Formulare
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    criteria Fulfill
    Item
    meets 1 of the following criteria:
    boolean
    C0243161 (UMLS CUI [1,1])
    C1550543 (UMLS CUI [1,2])
    Gender | Breast Carcinoma | Excision Planned
    Item
    women with breast tumors planning to undergo surgical resection
    boolean
    C0079399 (UMLS CUI [1])
    C0678222 (UMLS CUI [2])
    C0728940 (UMLS CUI [3,1])
    C1301732 (UMLS CUI [3,2])
    Healthy Volunteers | Well female adult | Breast Carcinoma
    Item
    healthy volunteers, including any constitutionally healthy female with no history of breast cancer
    boolean
    C1708335 (UMLS CUI [1])
    C0686752 (UMLS CUI [2])
    C0678222 (UMLS CUI [3])
    Hormone Receptor Status Unspecified
    Item
    hormone receptor status not specified
    boolean
    C0019929 (UMLS CUI [1,1])
    C0449438 (UMLS CUI [1,2])
    C0205370 (UMLS CUI [1,3])
    patient 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])
    Pregnancy | Breast Feeding
    Item
    not pregnant or nursing
    boolean
    C0032961 (UMLS CUI [1])
    C0006147 (UMLS CUI [2])
    Pregnancy test negative
    Item
    negative pregnancy test
    boolean
    C0427780 (UMLS CUI [1])
    Fertility Contraceptive methods
    Item
    fertile patients must use effective contraception
    boolean
    C0015895 (UMLS CUI [1,1])
    C0700589 (UMLS CUI [1,2])
    Illness
    Item
    not acutely ill
    boolean
    C0221423 (UMLS CUI [1])
    Foreign materials Magnetic metal Present Body
    Item
    no non-magnetic resonance-compatible ferromagnetic materials present in the body
    boolean
    C0016542 (UMLS CUI [1,1])
    C0439876 (UMLS CUI [1,2])
    C0150312 (UMLS CUI [1,3])
    C1268086 (UMLS CUI [1,4])
    concurrent therapy
    Item
    prior concurrent therapy:
    boolean
    C0009429 (UMLS CUI [1])
    Prior Chemotherapy | prior radiation therapy
    Item
    prior chemotherapy and/or radiotherapy allowed
    boolean
    C1514457 (UMLS CUI [1])
    C0279134 (UMLS CUI [2])
    Zum Seitenanfang zurückkehren 

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