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ID

23120

Beschreibung

Goserelin in Preventing Ovarian Failure in Women Receiving Chemotherapy for Breast Cancer https://clinicaltrials.gov/ct2/show/NCT00068601 Breast Cancer NCT00068601 Pre-Study - Southwest Oncology Group PreStudy (S0230) - 2170510v3.0

Link

https://clinicaltrials.gov/ct2/show/NCT00068601

Stichworte

  1. 26.08.12 26.08.12 -
  2. 24.06.17 24.06.17 - Martin Dugas
Hochgeladen am

24. Juni 2017

DOI

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Lizenz

Creative Commons BY 4.0

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    Breast Cancer Goserelin in Preventing Ovarian Failure NCT00068601 SWOG S0230

    Instructions: All dates are MONTH, DAY, YEAR. Explain any blank fields or blank dates in the Comments section.

    Disease Description
    Beschreibung

    Disease Description

    Alias
    UMLS CUI-1
    C3259023
    Date of Initial Diagnosis of Primary Tumor
    Beschreibung

    First Positive Biopsy Date

    Datentyp

    date

    Alias
    UMLS CUI [1]
    C4296634
    Stage
    Beschreibung

    Breast Tumor Stage

    Datentyp

    text

    Alias
    NCI Thesaurus ObjectClass
    C3262
    NCI Thesaurus ObjectClass-2
    C12971
    NCI Thesaurus ValueDomain
    C16899
    NCI Thesaurus Property
    C38027
    UMLS CUI [1,1]
    C1300072
    UMLS CUI [1,2]
    C0678222
    Date of last menses (Please fill in the following values if the Patient has not had regular menses within the past 6 weeks)
    Beschreibung

    last menstrual period

    Datentyp

    date

    Alias
    UMLS CUI [1]
    C0425932
    Laboratory Tests
    Beschreibung

    Laboratory Tests

    Alias
    UMLS CUI-1
    C0022885
    FSH level
    Beschreibung

    FSH value

    Datentyp

    float

    Maßeinheiten
    • IU/L
    Alias
    UMLS CUI [1]
    C0202022
    IU/L
    Laboratory lower limit for post menopausal FSH
    Beschreibung

    FSH LLN

    Datentyp

    float

    Maßeinheiten
    • IU/L
    Alias
    NCI Thesaurus ObjectClass
    C25294
    NCI Thesaurus Property
    C20200
    NCI Thesaurus Property-2
    C2286
    NCI Thesaurus ValueDomain
    C25712
    NCI Thesaurus ValueDomain-2
    C25555
    UMLS CUI [1,1]
    C0202022
    UMLS CUI [1,2]
    C1518030
    IU/L
    Estradiol level
    Beschreibung

    Estradiol

    Datentyp

    float

    Maßeinheiten
    • pg/mL
    Alias
    UMLS CUI [1]
    C0014912
    pg/mL
    Laboratory upper limit for post menopausal estradiol
    Beschreibung

    Estradiol ULN

    Datentyp

    float

    Maßeinheiten
    • pg/mL
    Alias
    UMLS CUI [1,1]
    C0014912
    UMLS CUI [1,2]
    C1519815
    pg/mL
    Planned Chemotherapy regimen (select one)
    Beschreibung

    Chemotherapy Type

    Datentyp

    integer

    Alias
    NCI Thesaurus ValueDomain
    C25284
    NCI Thesaurus ObjectClass
    C25320
    NCI Thesaurus ObjectClass-2
    C15632
    NCI Thesaurus Property
    C25382
    UMLS CUI [1,1]
    C0392920
    UMLS CUI [1,2]
    C1301732
    Other anthracycline-based regimen, specify chemotherapy agents and duration
    Beschreibung

    Other anthracycline-based regimen, specify

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C0282564
    UMLS CUI [1,2]
    C0205394
    CCRR Module For Southwest Oncology Group Prestudy (s0230)
    Beschreibung

    CCRR Module For Southwest Oncology Group Prestudy (s0230)

    Alias
    UMLS CUI-1
    C1320722
    SWOG Patient ID
    Beschreibung

    SWOG Patient ID (L, F, M)

    Datentyp

    text

    Alias
    NCI Thesaurus ValueDomain
    C25337
    NCI Thesaurus ObjectClass
    C16960
    NCI Thesaurus Property
    C25364
    NCI Thesaurus Property-2
    C25699
    UMLS CUI [1,1]
    C2348585
    UMLS CUI [1,2]
    C1519429
    Insitution/Affiliate
    Beschreibung

    Institution Name

    Datentyp

    text

    Alias
    NCI Thesaurus ObjectClass
    C25454
    NCI Thesaurus ObjectClass-2
    C21541
    NCI Thesaurus Property
    C25364
    NCI Thesaurus ValueDomain
    C25191
    NCI Thesaurus ValueDomain-2
    C21541
    UMLS CUI [1]
    C1301943
    Physician
    Beschreibung

    Registered Investigator Name

    Datentyp

    text

    Alias
    NCI Thesaurus ValueDomain
    C25191
    NCI Thesaurus Property
    C25364
    NCI Thesaurus ObjectClass
    C17089
    NCI Thesaurus ObjectClass-2
    C25644
    UMLS CUI [1]
    C2826892
    Group Name
    Beschreibung

    Participating Group Name

    Datentyp

    text

    Alias
    NCI Thesaurus ValueDomain
    C25191
    NCI Thesaurus ObjectClass
    C25608
    NCI Thesaurus ObjectClass-2
    C17005
    NCI Thesaurus Property
    C25364
    UMLS CUI [1]
    C2347449
    Study No.
    Beschreibung

    Protocol ID

    Datentyp

    text

    Alias
    NCI Thesaurus ValueDomain
    C25337
    NCI Thesaurus ObjectClass
    C25320
    NCI Thesaurus Property
    C25608
    NCI Thesaurus Property-2
    C25364
    UMLS CUI [1]
    C2826693
    Patient ID
    Beschreibung

    Patient Identifier Number

    Datentyp

    text

    Alias
    NCI Thesaurus ValueDomain
    C25337
    NCI Thesaurus ObjectClass
    C16960
    NCI Thesaurus Property
    C25608
    NCI Thesaurus Property-2
    C25364
    UMLS CUI [1]
    C2348585
    Height
    Beschreibung

    Patient Height

    Datentyp

    float

    Maßeinheiten
    • cm
    Alias
    NCI Thesaurus ValueDomain
    C25209
    NCI Thesaurus ObjectClass
    C16960
    NCI Thesaurus Property
    C25347
    UMLS CUI [1]
    C0489786
    cm
    Performance Status
    Beschreibung

    Performance Status

    Datentyp

    integer

    Alias
    UMLS CUI [1]
    C1520224

    Ähnliche Modelle

    Instructions: All dates are MONTH, DAY, YEAR. Explain any blank fields or blank dates in the Comments section.

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    Disease Description
    C3259023 (UMLS CUI-1)
    First Positive Biopsy Date
    Item
    Date of Initial Diagnosis of Primary Tumor
    date
    C4296634 (UMLS CUI [1])
    Item
    Stage
    text
    C3262 (NCI Thesaurus ObjectClass)
    C12971 (NCI Thesaurus ObjectClass-2)
    C16899 (NCI Thesaurus ValueDomain)
    C38027 (NCI Thesaurus Property)
    C1300072 (UMLS CUI [1,1])
    C0678222 (UMLS CUI [1,2])
    Code List
    Stage
    CL Item
    T1*, N0, M0 (I)
    CL Item
    Ii, According To Current AJCC Guidelines (II)
    CL Item
    T0, N2, M0 Or T1*, N2, M0 Or T2, N2, M0 Or T3, N1, M0 Or T3, N2, M0 (IIIA)
    last menstrual period
    Item
    Date of last menses (Please fill in the following values if the Patient has not had regular menses within the past 6 weeks)
    date
    C0425932 (UMLS CUI [1])
    Item Group
    Laboratory Tests
    C0022885 (UMLS CUI-1)
    FSH value
    Item
    FSH level
    float
    C0202022 (UMLS CUI [1])
    FSH LLN
    Item
    Laboratory lower limit for post menopausal FSH
    float
    C25294 (NCI Thesaurus ObjectClass)
    C20200 (NCI Thesaurus Property)
    C2286 (NCI Thesaurus Property-2)
    C25712 (NCI Thesaurus ValueDomain)
    C25555 (NCI Thesaurus ValueDomain-2)
    C0202022 (UMLS CUI [1,1])
    C1518030 (UMLS CUI [1,2])
    Estradiol
    Item
    Estradiol level
    float
    C0014912 (UMLS CUI [1])
    Estradiol ULN
    Item
    Laboratory upper limit for post menopausal estradiol
    float
    C0014912 (UMLS CUI [1,1])
    C1519815 (UMLS CUI [1,2])
    Item
    Planned Chemotherapy regimen (select one)
    integer
    C25284 (NCI Thesaurus ValueDomain)
    C25320 (NCI Thesaurus ObjectClass)
    C15632 (NCI Thesaurus ObjectClass-2)
    C25382 (NCI Thesaurus Property)
    C0392920 (UMLS CUI [1,1])
    C1301732 (UMLS CUI [1,2])
    Code List
    Planned Chemotherapy regimen (select one)
    CL Item
    AC (1)
    CL Item
    CAF (2)
    CL Item
    TAC (3)
    CL Item
    CEF (4)
    CL Item
    AC followed by a Taxane (5)
    Other anthracycline-based regimen, specify
    Item
    Other anthracycline-based regimen, specify chemotherapy agents and duration
    text
    C0282564 (UMLS CUI [1,1])
    C0205394 (UMLS CUI [1,2])
    Item Group
    CCRR Module For Southwest Oncology Group Prestudy (s0230)
    C1320722 (UMLS CUI-1)
    Southwest Oncology Group Identifier Number
    Item
    SWOG Patient ID
    text
    C25337 (NCI Thesaurus ValueDomain)
    C16960 (NCI Thesaurus ObjectClass)
    C25364 (NCI Thesaurus Property)
    C25699 (NCI Thesaurus Property-2)
    C2348585 (UMLS CUI [1,1])
    C1519429 (UMLS CUI [1,2])
    Institution Name
    Item
    Insitution/Affiliate
    text
    C25454 (NCI Thesaurus ObjectClass)
    C21541 (NCI Thesaurus ObjectClass-2)
    C25364 (NCI Thesaurus Property)
    C25191 (NCI Thesaurus ValueDomain)
    C21541 (NCI Thesaurus ValueDomain-2)
    C1301943 (UMLS CUI [1])
    Registered Investigator Name
    Item
    Physician
    text
    C25191 (NCI Thesaurus ValueDomain)
    C25364 (NCI Thesaurus Property)
    C17089 (NCI Thesaurus ObjectClass)
    C25644 (NCI Thesaurus ObjectClass-2)
    C2826892 (UMLS CUI [1])
    Participating Group Name
    Item
    Group Name
    text
    C25191 (NCI Thesaurus ValueDomain)
    C25608 (NCI Thesaurus ObjectClass)
    C17005 (NCI Thesaurus ObjectClass-2)
    C25364 (NCI Thesaurus Property)
    C2347449 (UMLS CUI [1])
    Protocol ID
    Item
    Study No.
    text
    C25337 (NCI Thesaurus ValueDomain)
    C25320 (NCI Thesaurus ObjectClass)
    C25608 (NCI Thesaurus Property)
    C25364 (NCI Thesaurus Property-2)
    C2826693 (UMLS CUI [1])
    Patient Identifier Number
    Item
    Patient ID
    text
    C25337 (NCI Thesaurus ValueDomain)
    C16960 (NCI Thesaurus ObjectClass)
    C25608 (NCI Thesaurus Property)
    C25364 (NCI Thesaurus Property-2)
    C2348585 (UMLS CUI [1])
    Patient Height
    Item
    Height
    float
    C25209 (NCI Thesaurus ValueDomain)
    C16960 (NCI Thesaurus ObjectClass)
    C25347 (NCI Thesaurus Property)
    C0489786 (UMLS CUI [1])
    Item
    Performance Status
    integer
    C1520224 (UMLS CUI [1])
    Code List
    Performance Status
    CL Item
    0 (0)
    C0919414 (NCI Metathesaurus)
    CL Item
    1 (1)
    CL Item
    2 (2)
    C66833 (NCI Thesaurus)
    C0205448 (UMLS 2011AA)
    CL Item
    3 (3)
    CL Item
    4 (4)

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