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1176

Description

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

Lien

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

Mots-clés

  1. 27/08/2012 27/08/2012 -
  2. 09/01/2015 09/01/2015 - Martin Dugas
Téléchargé le

27 août 2012

DOI

Pour une demande vous connecter.

Licence

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
    Description

    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.)
    Description

    IndicatewhichchemopreventionagentsthepatientreceivedBEFOREDIAGNOSISandindicatethenumberofmonthspatientreceivedtheseagents.

    Type de données

    text

    Other, specify (therapy)
    Description

    AgentName

    Type de données

    text

    Other, specify (therapy)
    Description

    AgentName

    Type de données

    text

    MONTHS
    Description

    MONTHS

    Type de données

    text

    DATE STOPPED (If continuing, use -1)
    Description

    AgentEndDate

    Type de données

    date

    Prior Chemotherapy Regimen For Breast Cancer
    Description

    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.)
    Description

    Didpatientreceiveadjuvantand/orneoadjuvantchemotherapyforbreastcancer?

    Type de données

    text

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

    PriorChemotherapyBeginDate

    Type de données

    date

    Other, specify (therapy)
    Description

    AgentName

    Type de données

    text

    Other, specify (therapy)
    Description

    AgentName

    Type de données

    text

    Other, specify (therapy)
    Description

    AgentName

    Type de données

    text

    Neoadjuvant Total Number of Cycles
    Description

    AgentCountCoursesAdministered

    Type de données

    double

    Neoadjuvant Total Number of Cycles
    Description

    AgentCountCoursesAdministered

    Type de données

    double

    DATE STOPPED (If continuing, use -1)
    Description

    AgentEndDate

    Type de données

    date

    Agent Dose
    Description

    AgentTotalDose

    Type de données

    double

    Agent Dose
    Description

    AgentTotalDose

    Type de données

    double

    Route
    Description

    AgentAdminRoute

    Type de données

    text

    Other SERM, (specify)
    Description

    OtherSERM,

    Type de données

    text

    DATE STARTED (D M Y)
    Description

    AgentBeginDate

    Type de données

    date

    Investigator/Designee Signature
    Description

    InvestigatorSignature

    Type de données

    text

    Alias
    NCI Thesaurus Property
    C25678
    UMLS 2011AA Property
    C1519316
    NCI Thesaurus ObjectClass
    C17089
    UMLS 2011AA ObjectClass
    C0035173
    Date (day month year)
    Description

    InvestigatorSignatureDate

    Type de données

    date

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

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

    Patient ID Number (Study No.)
    Description

    PatientStudyID,CoordinatingGroup

    Type de données

    text

    Patient Initials (f m fl sl)
    Description

    PatientInitialsName

    Type de données

    text

    Alias
    NCI Thesaurus ValueDomain
    C25191
    UMLS 2011AA ValueDomain
    C1547383
    NCI Thesaurus ObjectClass
    C16960
    UMLS 2011AA ObjectClass
    C0030705
    NCI Thesaurus Property
    C25536
    UMLS 2011AA Property
    C1555582
    Patient's Date of Birth (day)
    Description

    PatientBirthDate

    Type de données

    date

    Alias
    NCI Thesaurus ObjectClass
    C16960
    UMLS 2011AA ObjectClass
    C0030705
    NCI Thesaurus Property
    C25275
    UMLS 2011AA Property
    C2745955
    Participating Center/Affiliate
    Description

    MainMemberInstitution/Affiliate

    Type de données

    text

    Center Code (Ver.#1)
    Description

    ParticipatingGroupCode

    Type de données

    text

    Alias
    NCI Thesaurus ValueDomain
    C25162
    UMLS 2011AA ValueDomain
    C0805701

    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
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    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
    double
    AgentCountCoursesAdministered
    Item
    Neoadjuvant Total Number of Cycles
    double
    AgentEndDate
    Item
    DATE STOPPED (If continuing, use -1)
    date
    AgentTotalDose
    Item
    Agent Dose
    double
    AgentTotalDose
    Item
    Agent Dose
    double
    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
    PatientInitialsName
    Item
    Patient Initials (f m fl sl)
    text
    C25191 (NCI Thesaurus ValueDomain)
    C1547383 (UMLS 2011AA ValueDomain)
    C16960 (NCI Thesaurus ObjectClass)
    C0030705 (UMLS 2011AA ObjectClass)
    C25536 (NCI Thesaurus Property)
    C1555582 (UMLS 2011AA 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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