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ID

27861

Description

Study part: End of Study. 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.

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Versions (1)
  1. 12/3/17 12/3/17 -
Copyright Holder

Charité – University of medicine Berlin

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December 3, 2017

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Creative Commons BY-NC 3.0
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    End of Study SirTac NCT02936388

    German

    End of Study

    1 forms  
    1. StudyEvent: ODM
      1. End of Study
    Studienende
    Description

    Studienende

    Alias
    UMLS CUI-1
    C0008972
    UMLS CUI-2
    C0444930
    Patienten-ID:
    Description

    Patienten-ID

    Data type

    text

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

    Random. Nr.

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C1300638
    UMLS CUI [1,2]
    C0034656
    Studienende am
    Description

    study end date

    Data type

    date

    Alias
    UMLS CUI [1]
    C2983670
    Studienende
    Description

    study end

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0008972
    UMLS CUI [1,2]
    C0444930
    Gründe für unplanmäßiges Studienende:
    Description

    reason study end

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0444496
    UMLS CUI [1,2]
    C0392360
    Datum des Todes
    Description

    date of death

    Data type

    date

    Alias
    UMLS CUI [1]
    C1148348
    Todesursache:
    Description

    Cause of death

    Data type

    text

    Alias
    UMLS CUI [1]
    C0007465
    Therapiebedingte Komplikationen, welche
    Description

    Therapy complication

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0087111
    UMLS CUI [1,2]
    C0009566
    Andere Todesursache, welche
    Description

    other cause of death

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0205394
    UMLS CUI [1,2]
    C0007465
    Obduktion durchgeführt:
    Description

    Autopsy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0004398
    Patient/in nicht mehr erreichbar (lost to follow up)- Grund, falls bekannt
    Description

    reason lost to follow-up

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0566251
    UMLS CUI [1,2]
    C1302313
    Rücknahme der Einwilligung zur Studienteilnahme- Grund, falls bekannt
    Description

    Reason consent withdrawn

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0566251
    UMLS CUI [1,2]
    C1707492
    Anderer Grund für Studienende
    Description

    other reason study end

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0205394
    UMLS CUI [1,2]
    C0444496
    UMLS CUI [1,3]
    C0392360
    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

    End of Study

    1 forms
    1. StudyEvent: ODM
      1. End of Study
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Studienende
    C0008972 (UMLS CUI-1)
    C0444930 (UMLS CUI-2)
    Patienten-ID
    Item
    Patienten-ID:
    text
    C2348585 (UMLS CUI [1])
    Random. Nr.
    Item
    Random. Nr.:
    text
    C1300638 (UMLS CUI [1,1])
    C0034656 (UMLS CUI [1,2])
    study end date
    Item
    Studienende am
    date
    C2983670 (UMLS CUI [1])
    Item
    Studienende
    text
    C0008972 (UMLS CUI [1,1])
    C0444930 (UMLS CUI [1,2])
    study end
    Code List
    Studienende
    CL Item
    planmäßig (planmäßig)
    CL Item
    unplanmäßig (vorzeitig) (unplanmäßig (vorzeitig))
    Item
    Gründe für unplanmäßiges Studienende:
    text
    C0444496 (UMLS CUI [1,1])
    C0392360 (UMLS CUI [1,2])
    reason study end
    Code List
    Gründe für unplanmäßiges Studienende:
    CL Item
    Patient/in verstorben (Patient/in verstorben)
    C1306577 (UMLS CUI-1)
    (Comment:de)
    CL Item
    Patient/in nicht mehr erreichbar (lost to follow up) (Patient/in nicht mehr erreichbar (lost to follow up))
    C1302313 (UMLS CUI-1)
    (Comment:de)
    CL Item
    Rücknahme der Einwilligung zur Studienteilnahme (Rücknahme der Einwilligung zur Studienteilnahme)
    C1707492 (UMLS CUI-1)
    (Comment:de)
    CL Item
    Anderer Grund für Studienende (Anderer Grund für Studienende)
    C0205394 (UMLS CUI-1)
    (Comment:de)
    date of death
    Item
    Datum des Todes
    date
    C1148348 (UMLS CUI [1])
    Item
    Todesursache:
    text
    C0007465 (UMLS CUI [1])
    Cause of death
    Code List
    Todesursache:
    CL Item
    tumorbedingt – hepatischer Progress (tumorbedingt – hepatischer Progress)
    CL Item
    tumorbedingt – extrahepatischer Progress (tumorbedingt – extrahepatischer Progress)
    CL Item
    therapiebedingte Komplikationen (therapiebedingte Komplikationen)
    CL Item
    andere Todesursache (andere Todesursache)
    CL Item
    unbekannte Todesursache (unbekannte Todesursache)
    Therapy complication
    Item
    Therapiebedingte Komplikationen, welche
    text
    C0087111 (UMLS CUI [1,1])
    C0009566 (UMLS CUI [1,2])
    other cause of death
    Item
    Andere Todesursache, welche
    text
    C0205394 (UMLS CUI [1,1])
    C0007465 (UMLS CUI [1,2])
    Autopsy
    Item
    Obduktion durchgeführt:
    boolean
    C0004398 (UMLS CUI [1])
    reason lost to follow-up
    Item
    Patient/in nicht mehr erreichbar (lost to follow up)- Grund, falls bekannt
    text
    C0566251 (UMLS CUI [1,1])
    C1302313 (UMLS CUI [1,2])
    Reason consent withdrawn
    Item
    Rücknahme der Einwilligung zur Studienteilnahme- Grund, falls bekannt
    text
    C0566251 (UMLS CUI [1,1])
    C1707492 (UMLS CUI [1,2])
    other reason study end
    Item
    Anderer Grund für Studienende
    text
    C0205394 (UMLS CUI [1,1])
    C0444496 (UMLS CUI [1,2])
    C0392360 (UMLS CUI [1,3])
    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])
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