ID

14931

Beskrivning

International Collaborative Treatment Protocol For Children And Adolescents With Acute Lymphoblastic Leukemia. Phase 3 Study. Documentation part. Clinical Trial Number: NCT01117441.

Nyckelord

  1. 2016-05-09 2016-05-09 -
Uppladdad den

9 maj 2016

DOI

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Licens

Creative Commons BY-NC-ND 3.0

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    HR-2 therapy documentation AIEOP-BFM ALL 2009 DRKS00003772 NCT01117441

    HR-2 therapy documentation AIEOP-BFM ALL 2009 NCT01117441

    Patient Information
    Beskrivning

    Patient Information

    Alias
    UMLS CUI-1
    C1955348
    Stud.-Nr. (Pat.-ID)
    Beskrivning

    Patient ID

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C2348585
    Patient date of birth
    Beskrivning

    Patient birthday

    Datatyp

    date

    Alias
    UMLS CUI [1]
    C0421451
    Body weight
    Beskrivning

    Weight

    Datatyp

    float

    Måttenheter
    • kg
    Alias
    UMLS CUI [1]
    C0005910
    kg
    Body height
    Beskrivning

    Height

    Datatyp

    float

    Måttenheter
    • cm
    Alias
    UMLS CUI [1]
    C0005890
    cm
    Body surface
    Beskrivning

    Body surface

    Datatyp

    float

    Måttenheter
    • mˆ2
    Alias
    UMLS CUI [1]
    C0005902
    mˆ2
    Chemotherapy Regimen
    Beskrivning

    Chemotherapy Regimen

    Alias
    UMLS CUI-1
    C0392920
    Dexamethasone administration form
    Beskrivning

    Dexamethasone: administration form

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C0011777
    UMLS CUI [1,2]
    C0013153
    Dexamethasone dosage 20 mg/mˆ2/d
    Beskrivning

    Dexamethasone: dosage

    Datatyp

    float

    Måttenheter
    • mg
    Alias
    UMLS CUI [1,1]
    C0011777
    UMLS CUI [1,2]
    C0178602
    mg
    Dexamethasone Date of administration
    Beskrivning

    Dexamethasone: date of administration

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0011777
    UMLS CUI [1,2]
    C2584899
    VDS administration form i.v.
    Beskrivning

    VDS: administration form

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0042682
    UMLS CUI [1,2]
    C1522726
    VDS dosage (max. 5 mg) 3 mg/mˆ2/ED
    Beskrivning

    VDS: dosage

    Datatyp

    float

    Måttenheter
    • mg
    Alias
    UMLS CUI [1,1]
    C0042682
    UMLS CUI [1,2]
    C0178602
    mg
    VDS Date of administration
    Beskrivning

    VDS: date of administration

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0042682
    UMLS CUI [1,2]
    C2584899
    DNR administration form p.i. (24h)
    Beskrivning

    DNR: administration form

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0011015
    UMLS CUI [1,2]
    C1827465
    DNR dosage 30 mg/mˆ2/ED
    Beskrivning

    DNR: dosage

    Datatyp

    float

    Måttenheter
    • mg
    Alias
    UMLS CUI [1,1]
    C0011015
    UMLS CUI [1,2]
    C0178602
    mg
    DNR Date of administration
    Beskrivning

    DNR: date of administration

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0011015
    UMLS CUI [1,2]
    C2584899
    HD-MTX administration form p.i. (24h) (10% in 0,5 h, 90% in 23,5h)
    Beskrivning

    HD-MTX: administration form

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0025677
    UMLS CUI [1,2]
    C0149710
    UMLS CUI [1,3]
    C1827465
    HD-MTX dosage 5000 mg/ˆ2
    Beskrivning

    HD-MTX: dosage

    Datatyp

    float

    Måttenheter
    • mg
    Alias
    UMLS CUI [1,1]
    C0025677
    UMLS CUI [1,2]
    C0149710
    UMLS CUI [1,3]
    C0178602
    mg
    HD-MTX Date of administration
    Beskrivning

    HD-MTX: date of administration

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0025677
    UMLS CUI [1,2]
    C0149710
    UMLS CUI [1,3]
    C2584899
    LCV-Rescue administration form i.v.
    Beskrivning

    LCV-Rescue: administration form

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0023413
    UMLS CUI [1,2]
    C1522726
    LCV-rescue dosage 15 mg/ˆ2
    Beskrivning

    LCV-rescue: dosage

    Datatyp

    float

    Måttenheter
    • mg/ED
    Alias
    UMLS CUI [1,1]
    C0023413
    UMLS CUI [1,2]
    C0178602
    mg/ED
    LCV-rescue Date of administration (at hour 42, 48, 54)
    Beskrivning

    LCV-rescue: date of administration

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0023413
    UMLS CUI [1,2]
    C2584899
    CPM administration form p.i. (1h)
    Beskrivning

    IFO: administration form

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0020823
    UMLS CUI [1,2]
    C1827465
    IFO dosage 800 mg/mˆ2/ED (with MESNA: 300 mg/mˆ2 at hour 0, 4 and 8 of IFO infusion)
    Beskrivning

    IFO: dosage

    Datatyp

    float

    Måttenheter
    • mg
    Alias
    UMLS CUI [1,1]
    C0020823
    UMLS CUI [1,2]
    C0178602
    mg
    IFO Date of administration
    Beskrivning

    IFO: date of administration

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0020823
    UMLS CUI [1,2]
    C2584899
    PEG-L-ASP administration form p.i. (2h)
    Beskrivning

    PEG-L-ASP: administration form

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0071568
    UMLS CUI [1,2]
    C1827465
    PEG-L-ASP dosage 2500 mg/mˆ2/ED (ONCASPAR: 3750 E/ED)
    Beskrivning

    PEG-L-ASP: dosage

    Datatyp

    float

    Måttenheter
    • E
    Alias
    UMLS CUI [1,1]
    C0071568
    UMLS CUI [1,2]
    C0178602
    E
    PEG-L-ASP Date of administration
    Beskrivning

    PEG-L-ASP: date of administration

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0071568
    UMLS CUI [1,2]
    C2584899
    MTX administration form i.th
    Beskrivning

    MTX: administration form

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0025677
    UMLS CUI [1,2]
    C0677897
    MTX dosage (Age-dependent: 1 - < 2 y/o: 8 mg 2 - < 3y/o: 10 mg >= 3 y/o: 12 mg
    Beskrivning

    MTX: dosage

    Datatyp

    float

    Måttenheter
    • mg
    Alias
    UMLS CUI [1,1]
    C0025677
    UMLS CUI [1,2]
    C0178602
    mg
    MTX Date of administration (while MTX infusion)
    Beskrivning

    MTX: date of administration

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0025677
    UMLS CUI [1,2]
    C2584899
    If CNS leukemia, extra MTX dose (while MTX infusion): Date of administration
    Beskrivning

    MTX and CNS leukemia: date of administration

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0025677
    UMLS CUI [1,2]
    C1332884
    UMLS CUI [1,3]
    C2584899
    PEG-L-ASP/ Erwinase
    Beskrivning

    PEG-L-ASP/ Erwinase

    Alias
    UMLS CUI-1
    C0071568
    UMLS CUI-3
    C0591457
    Change from PEG-L-ASP to Erwinase in this element
    Beskrivning

    Change from PEG-L-ASP to Erwinase

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0580105
    UMLS CUI [1,2]
    C0071568
    UMLS CUI [1,3]
    C0591457
    If "yes", specify: Erwinase: date of first administration
    Beskrivning

    Erwinase: date of first administration

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0591457
    UMLS CUI [1,2]
    C2584899
    UMLS CUI [1,3]
    C0205435
    If "yes", specify: Erwinase: date of last administration
    Beskrivning

    Erwinase: date of last administration

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0591457
    UMLS CUI [1,2]
    C2584899
    UMLS CUI [1,3]
    C1517741
    If "yes", specify: Numbers of Erwinase doses
    Beskrivning

    Numbers of Erwinase doses

    Datatyp

    float

    Alias
    UMLS CUI [1,1]
    C0591457
    UMLS CUI [1,2]
    C0237753
    If "yes", specify: Reason for change to erwinase: Hypersensitivity
    Beskrivning

    Reason for drug change: Hypersensitivity

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0591457
    UMLS CUI [1,2]
    C0392747
    UMLS CUI [2]
    C0020517
    If "yes", specify: Reason for change to erwinase: Date of allergic reaction
    Beskrivning

    Reason for drug change: date of hypersensitivity

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0591457
    UMLS CUI [1,2]
    C0392747
    UMLS CUI [2,1]
    C0020517
    UMLS CUI [2,2]
    C0011008
    If "yes", specify: Reason for change to erwinase: Other reason
    Beskrivning

    Reason for drug change: Other reason

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C0591457
    UMLS CUI [1,2]
    C0392747
    UMLS CUI [2]
    C3840932
    Identification and Signature
    Beskrivning

    Identification and Signature

    Alias
    UMLS CUI-1
    C0205396
    UMLS CUI-3
    C1519316
    Date and signature of the doctor who calculated and created chemotherapy regimen
    Beskrivning

    Chemotherapy creator: signature

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C0392920
    UMLS CUI [1,2]
    C1707531
    UMLS CUI [2]
    C1519316
    Date and signature of the person who administered chemotherapy
    Beskrivning

    Chemotherapy administration: signature

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C0392920
    UMLS CUI [1,2]
    C1533734
    UMLS CUI [2]
    C1519316

    Similar models

    HR-2 therapy documentation AIEOP-BFM ALL 2009 NCT01117441

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    Patient Information
    C1955348 (UMLS CUI-1)
    Patient ID
    Item
    Stud.-Nr. (Pat.-ID)
    text
    C2348585 (UMLS CUI [1])
    Patient birthday
    Item
    Patient date of birth
    date
    C0421451 (UMLS CUI [1])
    Weight
    Item
    Body weight
    float
    C0005910 (UMLS CUI [1])
    Height
    Item
    Body height
    float
    C0005890 (UMLS CUI [1])
    Body surface
    Item
    Body surface
    float
    C0005902 (UMLS CUI [1])
    Item Group
    Chemotherapy Regimen
    C0392920 (UMLS CUI-1)
    Item
    Dexamethasone administration form
    text
    C0011777 (UMLS CUI [1,1])
    C0013153 (UMLS CUI [1,2])
    Code List
    Dexamethasone administration form
    CL Item
    p.o (p.o)
    CL Item
    i.v. (i.v.)
    Dexamethasone: dosage
    Item
    Dexamethasone dosage 20 mg/mˆ2/d
    float
    C0011777 (UMLS CUI [1,1])
    C0178602 (UMLS CUI [1,2])
    Dexamethasone: date of administration
    Item
    Dexamethasone Date of administration
    date
    C0011777 (UMLS CUI [1,1])
    C2584899 (UMLS CUI [1,2])
    VDS: administration form
    Item
    VDS administration form i.v.
    boolean
    C0042682 (UMLS CUI [1,1])
    C1522726 (UMLS CUI [1,2])
    VDS: dosage
    Item
    VDS dosage (max. 5 mg) 3 mg/mˆ2/ED
    float
    C0042682 (UMLS CUI [1,1])
    C0178602 (UMLS CUI [1,2])
    VDS: date of administration
    Item
    VDS Date of administration
    date
    C0042682 (UMLS CUI [1,1])
    C2584899 (UMLS CUI [1,2])
    DNR: administration form
    Item
    DNR administration form p.i. (24h)
    boolean
    C0011015 (UMLS CUI [1,1])
    C1827465 (UMLS CUI [1,2])
    DNR: dosage
    Item
    DNR dosage 30 mg/mˆ2/ED
    float
    C0011015 (UMLS CUI [1,1])
    C0178602 (UMLS CUI [1,2])
    DNR: date of administration
    Item
    DNR Date of administration
    date
    C0011015 (UMLS CUI [1,1])
    C2584899 (UMLS CUI [1,2])
    HD-MTX: administration form
    Item
    HD-MTX administration form p.i. (24h) (10% in 0,5 h, 90% in 23,5h)
    boolean
    C0025677 (UMLS CUI [1,1])
    C0149710 (UMLS CUI [1,2])
    C1827465 (UMLS CUI [1,3])
    HD-MTX: dosage
    Item
    HD-MTX dosage 5000 mg/ˆ2
    float
    C0025677 (UMLS CUI [1,1])
    C0149710 (UMLS CUI [1,2])
    C0178602 (UMLS CUI [1,3])
    HD-MTX: date of administration
    Item
    HD-MTX Date of administration
    date
    C0025677 (UMLS CUI [1,1])
    C0149710 (UMLS CUI [1,2])
    C2584899 (UMLS CUI [1,3])
    LCV-Rescue: administration form
    Item
    LCV-Rescue administration form i.v.
    boolean
    C0023413 (UMLS CUI [1,1])
    C1522726 (UMLS CUI [1,2])
    LCV-rescue: dosage
    Item
    LCV-rescue dosage 15 mg/ˆ2
    float
    C0023413 (UMLS CUI [1,1])
    C0178602 (UMLS CUI [1,2])
    LCV-rescue: date of administration
    Item
    LCV-rescue Date of administration (at hour 42, 48, 54)
    date
    C0023413 (UMLS CUI [1,1])
    C2584899 (UMLS CUI [1,2])
    IFO: administration form
    Item
    CPM administration form p.i. (1h)
    boolean
    C0020823 (UMLS CUI [1,1])
    C1827465 (UMLS CUI [1,2])
    IFO: dosage
    Item
    IFO dosage 800 mg/mˆ2/ED (with MESNA: 300 mg/mˆ2 at hour 0, 4 and 8 of IFO infusion)
    float
    C0020823 (UMLS CUI [1,1])
    C0178602 (UMLS CUI [1,2])
    IFO: date of administration
    Item
    IFO Date of administration
    date
    C0020823 (UMLS CUI [1,1])
    C2584899 (UMLS CUI [1,2])
    PEG-L-ASP: administration form
    Item
    PEG-L-ASP administration form p.i. (2h)
    boolean
    C0071568 (UMLS CUI [1,1])
    C1827465 (UMLS CUI [1,2])
    PEG-L-ASP: dosage
    Item
    PEG-L-ASP dosage 2500 mg/mˆ2/ED (ONCASPAR: 3750 E/ED)
    float
    C0071568 (UMLS CUI [1,1])
    C0178602 (UMLS CUI [1,2])
    PEG-L-ASP: date of administration
    Item
    PEG-L-ASP Date of administration
    date
    C0071568 (UMLS CUI [1,1])
    C2584899 (UMLS CUI [1,2])
    MTX: administration form
    Item
    MTX administration form i.th
    boolean
    C0025677 (UMLS CUI [1,1])
    C0677897 (UMLS CUI [1,2])
    MTX: dosage
    Item
    MTX dosage (Age-dependent: 1 - < 2 y/o: 8 mg 2 - < 3y/o: 10 mg >= 3 y/o: 12 mg
    float
    C0025677 (UMLS CUI [1,1])
    C0178602 (UMLS CUI [1,2])
    MTX: date of administration
    Item
    MTX Date of administration (while MTX infusion)
    date
    C0025677 (UMLS CUI [1,1])
    C2584899 (UMLS CUI [1,2])
    MTX and CNS leukemia: date of administration
    Item
    If CNS leukemia, extra MTX dose (while MTX infusion): Date of administration
    date
    C0025677 (UMLS CUI [1,1])
    C1332884 (UMLS CUI [1,2])
    C2584899 (UMLS CUI [1,3])
    Item Group
    PEG-L-ASP/ Erwinase
    C0071568 (UMLS CUI-1)
    C0591457 (UMLS CUI-3)
    Change from PEG-L-ASP to Erwinase
    Item
    Change from PEG-L-ASP to Erwinase in this element
    boolean
    C0580105 (UMLS CUI [1,1])
    C0071568 (UMLS CUI [1,2])
    C0591457 (UMLS CUI [1,3])
    Erwinase: date of first administration
    Item
    If "yes", specify: Erwinase: date of first administration
    date
    C0591457 (UMLS CUI [1,1])
    C2584899 (UMLS CUI [1,2])
    C0205435 (UMLS CUI [1,3])
    Erwinase: date of last administration
    Item
    If "yes", specify: Erwinase: date of last administration
    date
    C0591457 (UMLS CUI [1,1])
    C2584899 (UMLS CUI [1,2])
    C1517741 (UMLS CUI [1,3])
    Numbers of Erwinase doses
    Item
    If "yes", specify: Numbers of Erwinase doses
    float
    C0591457 (UMLS CUI [1,1])
    C0237753 (UMLS CUI [1,2])
    Reason for drug change: Hypersensitivity
    Item
    If "yes", specify: Reason for change to erwinase: Hypersensitivity
    boolean
    C0591457 (UMLS CUI [1,1])
    C0392747 (UMLS CUI [1,2])
    C0020517 (UMLS CUI [2])
    Reason for drug change: date of hypersensitivity
    Item
    If "yes", specify: Reason for change to erwinase: Date of allergic reaction
    date
    C0591457 (UMLS CUI [1,1])
    C0392747 (UMLS CUI [1,2])
    C0020517 (UMLS CUI [2,1])
    C0011008 (UMLS CUI [2,2])
    Reason for drug change: Other reason
    Item
    If "yes", specify: Reason for change to erwinase: Other reason
    text
    C0591457 (UMLS CUI [1,1])
    C0392747 (UMLS CUI [1,2])
    C3840932 (UMLS CUI [2])
    Item Group
    Identification and Signature
    C0205396 (UMLS CUI-1)
    C1519316 (UMLS CUI-3)
    Chemotherapy creator: signature
    Item
    Date and signature of the doctor who calculated and created chemotherapy regimen
    text
    C0392920 (UMLS CUI [1,1])
    C1707531 (UMLS CUI [1,2])
    C1519316 (UMLS CUI [2])
    Chemotherapy administration: signature
    Item
    Date and signature of the person who administered chemotherapy
    text
    C0392920 (UMLS CUI [1,1])
    C1533734 (UMLS CUI [1,2])
    C1519316 (UMLS CUI [2])

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