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9118

Descrizione

Prior Treatment History Form (Form 24-H) Brain Function in Premenopausal Women Receiving Tamoxifen With or Without Ovarian Function Suppression for Early-Stage Breast Cancer on Clinical Trial IBCSG-2402 Source Form: NCI FormBuilder: https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=B1274765-836E-53AF-E034-0003BA12F5E7

collegamento

https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=B1274765-836E-53AF-E034-0003BA12F5E7

Keywords

  1. 27/08/12 27/08/12 -
  2. 09/01/15 09/01/15 - Martin Dugas
Caricato su

9 gennaio 2015

DOI

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Licenza

Creative Commons BY-NC 3.0 Legacy

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    Breast Cancer NCT00659373 Pre-Study - Prior Treatment History Form (Form 24-H) - 2074666v3.0

    PRIOR TREATMENT HISTORY FORM (Form 24-H) Instructions: This form collects data on treatment of breast cancer prior to randomization. Please submit within one (1) month of randomization. Use minus one (-1) to indicate that an answer is unknown, unobtainable, or not done.

    Before Diagnosis: Chemoprevention For Breast Cancer
    Descrizione

    Before Diagnosis: Chemoprevention For Breast Cancer

    Indicate which chemoprevention agents the patient received BEFORE DIAGNOSIS and indicate the number of months patient received these agents. (select all that apply by marking an ?X? in the appropriate Therapy.)
    Descrizione

    IndicatewhichchemopreventionagentsthepatientreceivedBEFOREDIAGNOSISandindicatethenumberofmonthspatientreceivedtheseagents.

    Tipo di dati

    text

    Other, specify (therapy)
    Descrizione

    AgentName

    Tipo di dati

    text

    Other, specify (therapy)
    Descrizione

    AgentName

    Tipo di dati

    text

    MONTHS
    Descrizione

    MONTHS

    Tipo di dati

    text

    DATE STOPPED (If continuing, use -1)
    Descrizione

    AgentEndDate

    Tipo di dati

    date

    Prior Chemotherapy Regimen For Breast Cancer
    Descrizione

    Prior Chemotherapy Regimen For Breast Cancer

    Did patient receive adjuvant and/or neoadjuvant chemotherapy for breast cancer? (Mark your selection with an ?X? in the appropriate boxes.)
    Descrizione

    Didpatientreceiveadjuvantand/orneoadjuvantchemotherapyforbreastcancer?

    Tipo di dati

    text

    Date of first dose of chemotherapy (day month year)
    Descrizione

    PriorChemotherapyBeginDate

    Tipo di dati

    date

    Other, specify (therapy)
    Descrizione

    AgentName

    Tipo di dati

    text

    Other, specify (therapy)
    Descrizione

    AgentName

    Tipo di dati

    text

    Other, specify (therapy)
    Descrizione

    AgentName

    Tipo di dati

    text

    Neoadjuvant Total Number of Cycles
    Descrizione

    AgentCountCoursesAdministered

    Tipo di dati

    float

    Neoadjuvant Total Number of Cycles
    Descrizione

    AgentCountCoursesAdministered

    Tipo di dati

    float

    DATE STOPPED (If continuing, use -1)
    Descrizione

    AgentEndDate

    Tipo di dati

    date

    Agent Dose
    Descrizione

    AgentTotalDose

    Tipo di dati

    float

    Agent Dose
    Descrizione

    AgentTotalDose

    Tipo di dati

    float

    Route
    Descrizione

    AgentAdminRoute

    Tipo di dati

    text

    Other SERM, (specify)
    Descrizione

    OtherSERM,

    Tipo di dati

    text

    DATE STARTED (D M Y)
    Descrizione

    AgentBeginDate

    Tipo di dati

    date

    Investigator/Designee Signature
    Descrizione

    InvestigatorSignature

    Tipo di dati

    text

    Alias
    NCI Thesaurus Property
    C25678 (undefined)
    UMLS 2011AA Property
    C1519316 (Signature)
    LOINC
    LP248948-4
    NCI Thesaurus ObjectClass
    C17089 (undefined)
    UMLS 2011AA ObjectClass
    C0035173 (Research Personnel)
    SNOMED
    769038007
    LOINC
    LA23773-7
    Date (day month year)
    Descrizione

    InvestigatorSignatureDate

    Tipo di dati

    date

    Ccrr Module For Prior Treatment History Form (form 24-h)
    Descrizione

    Ccrr Module For Prior Treatment History Form (form 24-h)

    Patient ID Number (Study No.)
    Descrizione

    PatientStudyID,CoordinatingGroup

    Tipo di dati

    text

    Patient Initials (f m fl sl)
    Descrizione

    Patient Initials

    Tipo di dati

    text

    Alias
    NCI Thesaurus ValueDomain
    C25191 (undefined)
    UMLS CUI-1
    C2986440 (Person Initials)
    NCI Thesaurus ObjectClass
    C16960 (undefined)
    NCI Thesaurus Property
    C25536 (undefined)
    Patient's Date of Birth (day)
    Descrizione

    PatientBirthDate

    Tipo di dati

    date

    Alias
    NCI Thesaurus ObjectClass
    C16960 (undefined)
    UMLS 2011AA ObjectClass
    C0030705 (Patients)
    SNOMED
    116154003
    NCI Thesaurus Property
    C25275 (undefined)
    UMLS 2011AA Property
    C2745955 (Occurrence)
    SNOMED
    246454002
    Participating Center/Affiliate
    Descrizione

    MainMemberInstitution/Affiliate

    Tipo di dati

    text

    Center Code (Ver.#1)
    Descrizione

    ParticipatingGroupCode

    Tipo di dati

    text

    Alias
    NCI Thesaurus ValueDomain
    C25162 (undefined)
    UMLS 2011AA ValueDomain
    C0805701 (Code)

    Similar models

    PRIOR TREATMENT HISTORY FORM (Form 24-H) Instructions: This form collects data on treatment of breast cancer prior to randomization. Please submit within one (1) month of randomization. Use minus one (-1) to indicate that an answer is unknown, unobtainable, or not done.

    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    Alias
    Item Group
    Before Diagnosis: Chemoprevention For Breast Cancer
    IndicatewhichchemopreventionagentsthepatientreceivedBEFOREDIAGNOSISandindicatethenumberofmonthspatientreceivedtheseagents.
    Item
    Indicate which chemoprevention agents the patient received BEFORE DIAGNOSIS and indicate the number of months patient received these agents. (select all that apply by marking an ?X? in the appropriate Therapy.)
    text
    AgentName
    Item
    Other, specify (therapy)
    text
    AgentName
    Item
    Other, specify (therapy)
    text
    MONTHS
    Item
    MONTHS
    text
    AgentEndDate
    Item
    DATE STOPPED (If continuing, use -1)
    date
    Item Group
    Prior Chemotherapy Regimen For Breast Cancer
    Item
    Did patient receive adjuvant and/or neoadjuvant chemotherapy for breast cancer? (Mark your selection with an ?X? in the appropriate boxes.)
    text
    Code List
    Did patient receive adjuvant and/or neoadjuvant chemotherapy for breast cancer? (Mark your selection with an ?X? in the appropriate boxes.)
    CL Item
    No (No)
    C49487 (NCI Thesaurus)
    C1298908 (UMLS 2011AA)
    CL Item
    Neoadjuvant Only (Neoadjuvant only)
    CL Item
    Adjuvant Only (Adjuvant only)
    CL Item
    Both Adjuvant And Neoadjuvant (Both adjuvant and neoadjuvant)
    PriorChemotherapyBeginDate
    Item
    Date of first dose of chemotherapy (day month year)
    date
    AgentName
    Item
    Other, specify (therapy)
    text
    AgentName
    Item
    Other, specify (therapy)
    text
    AgentName
    Item
    Other, specify (therapy)
    text
    AgentCountCoursesAdministered
    Item
    Neoadjuvant Total Number of Cycles
    float
    AgentCountCoursesAdministered
    Item
    Neoadjuvant Total Number of Cycles
    float
    AgentEndDate
    Item
    DATE STOPPED (If continuing, use -1)
    date
    AgentTotalDose
    Item
    Agent Dose
    float
    AgentTotalDose
    Item
    Agent Dose
    float
    AgentAdminRoute
    Item
    Route
    text
    OtherSERM,
    Item
    Other SERM, (specify)
    text
    AgentBeginDate
    Item
    DATE STARTED (D M Y)
    date
    InvestigatorSignature
    Item
    Investigator/Designee Signature
    text
    C25678 (NCI Thesaurus Property)
    C1519316 (UMLS 2011AA Property)
    C17089 (NCI Thesaurus ObjectClass)
    C0035173 (UMLS 2011AA ObjectClass)
    InvestigatorSignatureDate
    Item
    Date (day month year)
    date
    Item Group
    Ccrr Module For Prior Treatment History Form (form 24-h)
    PatientStudyID,CoordinatingGroup
    Item
    Patient ID Number (Study No.)
    text
    Patient Initials
    Item
    Patient Initials (f m fl sl)
    text
    C25191 (NCI Thesaurus ValueDomain)
    C2986440 (UMLS CUI-1)
    C16960 (NCI Thesaurus ObjectClass)
    C25536 (NCI Thesaurus Property)
    PatientBirthDate
    Item
    Patient's Date of Birth (day)
    date
    C16960 (NCI Thesaurus ObjectClass)
    C0030705 (UMLS 2011AA ObjectClass)
    C25275 (NCI Thesaurus Property)
    C2745955 (UMLS 2011AA Property)
    MainMemberInstitution/Affiliate
    Item
    Participating Center/Affiliate
    text
    ParticipatingGroupCode
    Item
    Center Code (Ver.#1)
    text
    C25162 (NCI Thesaurus ValueDomain)
    C0805701 (UMLS 2011AA ValueDomain)

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