0 Ratings

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.

Keywords

  1. 12/3/17 12/3/17 -
Copyright Holder

Charité – University of medicine Berlin

Uploaded on

December 3, 2017

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :


    No comments

    In order to download data models you must be logged in. Please log in or register for free.

    End of Study SirTac NCT02936388

    End of Study

    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

    Similar models

    End of Study

    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])
    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])
    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])
    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])

    Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

    Watch Tutorial