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ID

18876

Description

Phase I study of panobinostat and imatinib in patients with treatment-refractory metastatic gastrointestinal stromal tumors WTZ-GIST-09-01 (EudraCT number: 2009-011417-24; German Clinical Trials Register: DRKS00000657) was approved by the institutional ethics committees of the two participating centers and the German Federal Regulatory Drug Agency (BfArM; 4035954).

Mots-clés

  1. 20/11/2016 20/11/2016 -
  2. 23/11/2016 23/11/2016 -
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23 novembre 2016

DOI

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Licence

Creative Commons BY-NC-ND 3.0

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    WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 1 Week 1 (V2) 2009-011417-24 DRKS00000657

    WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 1 Week 1 (V2) 2009-011417-24

    Vital signs
    Description

    Vital signs

    Alias
    UMLS CUI-1
    C0518766
    Start of cycle
    Description

    Start of cycle

    Type de données

    date

    Unités de mesure
    • YYYY-MM-DD
    Alias
    UMLS CUI [1,1]
    C0808070
    UMLS CUI [1,2]
    C1302181
    YYYY-MM-DD
    Patient is eligible (all inclusion criteria are met and no exclusion criterion is met)
    Description

    Eligibility

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0013893
    Weight
    Description

    Weight

    Type de données

    float

    Alias
    UMLS CUI [1]
    C0005910
    Systolic blood pressure
    Description

    Systolic blood pressure

    Type de données

    integer

    Unités de mesure
    • mmHg
    Alias
    UMLS CUI [1]
    C0871470
    mmHg
    Diastolic blood pressure
    Description

    Diastolic blood pressure

    Type de données

    integer

    Unités de mesure
    • mmHg
    Alias
    UMLS CUI [1]
    C0428883
    mmHg
    pulse
    Description

    Heart rate

    Type de données

    integer

    Unités de mesure
    • Beats/Min
    Alias
    UMLS CUI [1]
    C0018810
    Beats/Min
    Temperature
    Description

    Body temperature

    Type de données

    float

    Unités de mesure
    • °C
    Alias
    UMLS CUI [1]
    C0005903
    °C
    ECG
    Description

    ECG

    Type de données

    integer

    Alias
    UMLS CUI [1]
    C1623258
    Physical examination
    Description

    Physical examination

    Type de données

    integer

    Alias
    UMLS CUI [1]
    C0031809
    Adverse events
    Description

    Adverse event

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0877248
    DLT
    Description

    Dose-limiting toxicity

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C1512043
    UMLS CUI [1,2]
    C0013221
    Concomitant medications
    Description

    Concomitant medications

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C2347852
    ECOG Status
    Description

    ECOG Status

    Type de données

    integer

    Alias
    UMLS CUI [1]
    C1520224

    Similar models

    WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 1 Week 1 (V2) 2009-011417-24

    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Vital signs
    C0518766 (UMLS CUI-1)
    Start of cycle
    Item
    Start of cycle
    date
    C0808070 (UMLS CUI [1,1])
    C1302181 (UMLS CUI [1,2])
    Eligibility
    Item
    Patient is eligible (all inclusion criteria are met and no exclusion criterion is met)
    boolean
    C0013893 (UMLS CUI [1])
    Weight
    Item
    Weight
    float
    C0005910 (UMLS CUI [1])
    Systolic blood pressure
    Item
    Systolic blood pressure
    integer
    C0871470 (UMLS CUI [1])
    Diastolic blood pressure
    Item
    Diastolic blood pressure
    integer
    C0428883 (UMLS CUI [1])
    Heart rate
    Item
    pulse
    integer
    C0018810 (UMLS CUI [1])
    Body temperature
    Item
    Temperature
    float
    C0005903 (UMLS CUI [1])
    Item
    ECG
    integer
    C1623258 (UMLS CUI [1])
    Code List
    ECG
    CL Item
    normal (0)
    CL Item
    out of range NCS (1)
    CL Item
    out of range (2)
    Item
    Physical examination
    integer
    C0031809 (UMLS CUI [1])
    Code List
    Physical examination
    CL Item
    normal (0)
    CL Item
    out of range NCS (1)
    CL Item
    out of range (2)
    Adverse event
    Item
    Adverse events
    boolean
    C0877248 (UMLS CUI [1])
    Dose-limiting toxicity
    Item
    DLT
    text
    C1512043 (UMLS CUI [1,1])
    C0013221 (UMLS CUI [1,2])
    Concomitant medications
    Item
    Concomitant medications
    boolean
    C2347852 (UMLS CUI [1])
    Item
    ECOG Status
    integer
    C1520224 (UMLS CUI [1])
    Code List
    ECOG Status
    CL Item
    Fully active (0)
    CL Item
    80-90% (1)
    CL Item
    60-70% (2)
    CL Item
    40-50% (3)
    CL Item
    10-30% (4)
    CL Item
    Dead (5)

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