ID

27764

Description

Study part: Follow- Up. A Randomized Phase II Trial of Transarterial Radioembolisation With Yttrium-90 (SIRT) in Comparison to Transarterial Chemoembolisation With Cisplatin (TACE) in Patients With Liver Metastases From Uveal Melanoma. Provided by Prof. Dr. Ulrich Keilholz, Charité – University of medicine Berlin. EudraCT-Nummer: 2014-002439-32. NCT02936388.

Keywords

Versions (1)
  1. 11/28/17 11/28/17 -
Copyright Holder

Charité – University of medicine Berlin

Uploaded on

November 28, 2017

DOI

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License

Creative Commons BY-NC 3.0
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    Follow- Up SirTac NCT02936388

    German

    Follow- Up

    1 forms  
    1. StudyEvent: ODM
      1. Follow- Up
    Follow- Up
    Description

    Follow- Up

    Alias
    UMLS CUI-1
    C1522577
    Patienten-ID:
    Description

    Patient-ID

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348585
    Random. Nr.:
    Description

    randomization number

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C1300638
    UMLS CUI [1,2]
    C0034656
    Follow-up Visite Nr.:
    Description

    visit number

    Data type

    integer

    Alias
    UMLS CUI [1]
    C1549755
    Durchgeführt am
    Description

    visit date

    Data type

    date

    Alias
    UMLS CUI [1]
    C1320303
    Allgemeiner Zustand:
    Description

    general condition

    Data type

    text

    Alias
    UMLS CUI [1]
    C1142435
    Krankheitsverlauf (Folgetherapien, relevante Ereignisse usw.):
    Description

    course of a disease

    Data type

    text

    Alias
    UMLS CUI [1]
    C0242656
    Späte Toxizitäten:
    Description

    Späte Toxizitäten:

    Alias
    UMLS CUI-1
    C0013221
    Code
    Description

    laut CTCAE-Kriterien

    Data type

    text

    Alias
    UMLS CUI [1]
    C0805701
    Art der Toxizität
    Description

    drug toxicity

    Data type

    text

    Alias
    UMLS CUI [1]
    C0013221
    Grad
    Description

    laut CTCAE-Kriterien

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0441800
    UMLS CUI [1,2]
    C0013221
    Keine Toxizität zu dokumentieren
    Description

    Documentation drug toxicity

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0920316
    UMLS CUI [1,2]
    C0013221
    Kommentar:
    Description

    comment

    Data type

    text

    Alias
    UMLS CUI [1]
    C0947611
    Ausgefüllt/bestätigt am:
    Description

    date

    Data type

    date

    Alias
    UMLS CUI [1]
    C0011008
    Name Prüfarzt
    Description

    investigator name

    Data type

    text

    Alias
    UMLS CUI [1]
    C2826892
    Unterschrift Prüfarzt
    Description

    investigator signature

    Data type

    text

    Alias
    UMLS CUI [1]
    C2346576
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    Similar models

    Follow- Up

    1 forms
    1. StudyEvent: ODM
      1. Follow- Up
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Follow- Up
    C1522577 (UMLS CUI-1)
    Patient-ID
    Item
    Patienten-ID:
    text
    C2348585 (UMLS CUI [1])
    randomization number
    Item
    Random. Nr.:
    text
    C1300638 (UMLS CUI [1,1])
    C0034656 (UMLS CUI [1,2])
    visit number
    Item
    Follow-up Visite Nr.:
    integer
    C1549755 (UMLS CUI [1])
    visit date
    Item
    Durchgeführt am
    date
    C1320303 (UMLS CUI [1])
    general condition
    Item
    Allgemeiner Zustand:
    text
    C1142435 (UMLS CUI [1])
    course of a disease
    Item
    Krankheitsverlauf (Folgetherapien, relevante Ereignisse usw.):
    text
    C0242656 (UMLS CUI [1])
    Item Group
    Späte Toxizitäten:
    C0013221 (UMLS CUI-1)
    Code
    Item
    Code
    text
    C0805701 (UMLS CUI [1])
    drug toxicity
    Item
    Art der Toxizität
    text
    C0013221 (UMLS CUI [1])
    Grade drug toxicity
    Item
    Grad
    text
    C0441800 (UMLS CUI [1,1])
    C0013221 (UMLS CUI [1,2])
    Documentation drug toxicity
    Item
    Keine Toxizität zu dokumentieren
    boolean
    C0920316 (UMLS CUI [1,1])
    C0013221 (UMLS CUI [1,2])
    comment
    Item
    Kommentar:
    text
    C0947611 (UMLS CUI [1])
    date
    Item
    Ausgefüllt/bestätigt am:
    date
    C0011008 (UMLS CUI [1])
    investigator name
    Item
    Name Prüfarzt
    text
    C2826892 (UMLS CUI [1])
    investigator signature
    Item
    Unterschrift Prüfarzt
    text
    C2346576 (UMLS CUI [1])
    Back to the top of the page 

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