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ID

31183

Beskrivning

Study ID: 104505 Clinical Study ID: BEX104505 Study Title: Phase II Study of Iodine 131 Anti B1 Antibody for 1st or 2nd Relapsed Indolent B-Cell Lymphomas or B-Cell Lymphomas That Have Transformed to a More Aggressive Histology Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00950755 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: tositumomab Trade Name: Bexxar Study Indication: Lymphoma, Non-Hodgkin Please record all concomitant medications and transfusions from the time of study entry through the Week 13 visit. Include study-required medications (i.e. Lugol's solution or potassium iodide, paracetamol, and diphenhydramine).

Nyckelord

Versioner (1)
  1. 2018-07-25 2018-07-25 -
Rättsinnehavare

see clinicaltrials.gov

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25 juli 2018

DOI

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Creative Commons BY 4.0
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    Iodine 131 B1 Antibody for B-Cell Lymphomas NCT00950755

    Engelsk

    Concomitant Medications & Transfusions

    1 Formulär  
    Administrative Data
    Beskrivning

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722 (Administrative documentation)
    SNOMED
    405624007
    Site Number
    Beskrivning

    Site number

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C0018704 (Health care facility)
    SNOMED
    257622000
    LOINC
    LA30302-6
    UMLS CUI [1,2]
    C0600091 (Identifier)
    SNOMED
    118522005
    LOINC
    LP31795-5
    Patient Number
    Beskrivning

    Patient Number

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C1830427 (undefined)
    Patient Initials
    Beskrivning

    Patient Initials

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C2986440 (Person Initials)
    Concomitant Medications; Concomitant Transfusions
    Beskrivning

    Concomitant Medications; Concomitant Transfusions

    Alias
    UMLS CUI-1
    C2347852 (Concomitant Agent)
    Drug Name or Blood Product
    Beskrivning

    Concomitant Agent; Drug Name or Blood Product

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C2347852 (Concomitant Agent)
    UMLS CUI [1,2]
    C2360065 (Medication name)
    LOINC
    MTHU027854
    UMLS CUI [1,3]
    C0456388 (Blood product)
    SNOMED
    410652009
    LOINC
    LP32808-5
    Dose
    Beskrivning

    Concomitant Agent; Dose

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C2347852 (Concomitant Agent)
    UMLS CUI [1,2]
    C3174092 (Medication dose)
    LOINC
    LP116765-1
    Unit
    Beskrivning

    Concomitant Agent; Unit

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C2347852 (Concomitant Agent)
    UMLS CUI [1,2]
    C1519795 (Unit of Measure)
    SNOMED
    767524001
    Route
    Beskrivning

    Concomitant Agent; Route

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C2347852 (Concomitant Agent)
    UMLS CUI [1,2]
    C0013153 (Drug Administration Routes)
    SNOMED
    410675002
    LOINC
    LP40261-7
    Frequency
    Beskrivning

    Concomitant Agent; Frequency

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C2347852 (Concomitant Agent)
    UMLS CUI [1,2]
    C3476109 (Medication frequency)
    LOINC
    LP149758-7
    Start Date
    Beskrivning

    Concomitant Agent; Start Date

    Datatyp

    date

    Alias
    UMLS CUI [1]
    C2826734 (Concomitant Medication Start Date)
    End Date
    Beskrivning

    Concomitant Agent; End Date

    Datatyp

    date

    Alias
    UMLS CUI [1]
    C2826744 (Concomitant Medication End Date)
    Tillbaka till toppen

    Similar models

    Concomitant Medications & Transfusions

    1 Formulär
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    Site number
    Item
    Site Number
    text
    C0018704 (UMLS CUI [1,1])
    C0600091 (UMLS CUI [1,2])
    Patient Number
    Item
    Patient Number
    text
    C1830427 (UMLS CUI [1])
    Patient Initials
    Item
    Patient Initials
    text
    C2986440 (UMLS CUI [1])
    Item Group
    Concomitant Medications; Concomitant Transfusions
    C2347852 (UMLS CUI-1)
    Concomitant Agent; Drug Name or Blood Product
    Item
    Drug Name or Blood Product
    text
    C2347852 (UMLS CUI [1,1])
    C2360065 (UMLS CUI [1,2])
    C0456388 (UMLS CUI [1,3])
    Concomitant Agent; Dose
    Item
    Dose
    text
    C2347852 (UMLS CUI [1,1])
    C3174092 (UMLS CUI [1,2])
    Concomitant Agent; Unit
    Item
    Unit
    text
    C2347852 (UMLS CUI [1,1])
    C1519795 (UMLS CUI [1,2])
    Concomitant Agent; Route
    Item
    Route
    text
    C2347852 (UMLS CUI [1,1])
    C0013153 (UMLS CUI [1,2])
    Concomitant Agent; Frequency
    Item
    Frequency
    text
    C2347852 (UMLS CUI [1,1])
    C3476109 (UMLS CUI [1,2])
    Concomitant Agent; Start Date
    Item
    Start Date
    date
    C2826734 (UMLS CUI [1])
    Concomitant Agent; End Date
    Item
    End Date
    date
    C2826744 (UMLS CUI [1])
    Tillbaka till toppen 

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