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ID

18897

Description

Positronen-Emissionstomographie-gesteuerte Therapie aggressiver Non-Hodgkin-Lymphome (PETAL-Studie) Universitätsklinikum Essen (UK Essen) EudraCT-Nummer: 2006-001641-33 NCT00554164

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  1. 11/23/16 11/23/16 -
  2. 11/23/16 11/23/16 -
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November 23, 2016

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Creative Commons BY-NC 3.0
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    End of study PETAL Study NCT00554164

    German English

    End of study

    1 forms  
    1. StudyEvent: ODM
      1. End of study
    Comorbidity
    Description

    Comorbidity

    Comorbidity number
    Description

    Comorbidity number

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0009488
    UMLS CUI [1,2]
    C0750480
    Comorbidity description
    Description

    Comorbidity description

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0678257
    UMLS CUI [1,2]
    C0009488
    Begin
    Description

    Begin

    Data type

    date

    Alias
    UMLS CUI [1]
    C0808070
    End
    Description

    End

    Data type

    date

    Measurement units
    • °C
    Alias
    UMLS CUI [1]
    C0806020
    °C
    Ongoing
    Description

    Ongoing

    Data type

    integer

    Alias
    UMLS CUI [1]
    C0549178
    Therapy
    Description

    Therapy

    Data type

    integer

    Alias
    UMLS CUI [1]
    C0087111
    Therapy begin
    Description

    Therapy begin

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0087111
    UMLS CUI [1,2]
    C0439659
    Therapy end
    Description

    Therapy end

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0087111
    UMLS CUI [1,2]
    C0444930
    Therapy ongoing
    Description

    Therapy ongoing

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0549178
    UMLS CUI [1,2]
    C0039798
    Discontinuation
    Description

    Discontinuation

    Alias
    UMLS CUI-1
    C0457454
    Death date
    Description

    Death date

    Data type

    date

    Alias
    UMLS CUI [1]
    C1148348
    Discontinuation date
    Description

    Discontinuation date

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C1444662
    UMLS CUI [1,2]
    C0011008
    Time of premature discontinuation
    Description

    Time of premature discontinuation

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0457454
    UMLS CUI [1,2]
    C0040223
    Reason for premature discontinuation of trial participation
    Description

    Reason for premature discontinuation of trial participation

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0457454
    UMLS CUI [1,2]
    C0392360
    Adverse event
    Description

    Adverse event

    Alias
    UMLS CUI-1
    C0877248
    Adverse event number
    Description

    Adverse event number

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0877248
    UMLS CUI [1,2]
    C0237753
    Begin
    Description

    Begin

    Data type

    date

    Alias
    UMLS CUI [1]
    C0808070
    End
    Description

    End

    Data type

    date

    Alias
    UMLS CUI [1]
    C0806020
    Adverse event
    Description

    Adverse event

    Data type

    text

    Alias
    UMLS CUI [1]
    C0877248
    Adverse event frequency
    Description

    Adverse event frequency

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0877248
    UMLS CUI [1,2]
    C0439603
    Adverse Event: Severity
    Description

    Adverse Event: Severity

    Data type

    integer

    Alias
    UMLS CUI [1]
    C1710066
    Adverse Event Action Code
    Description

    Adverse Event Action Code

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0877248
    UMLS CUI [1,2]
    C0441472
    UMLS CUI [1,3]
    C0805701
    Correlation with trial procedure
    Description

    Correlation with trial procedure

    Data type

    integer

    Alias
    UMLS CUI [1]
    C1707520
    Result of adverse event
    Description

    Result of adverse event

    Data type

    integer

    Alias
    UMLS CUI [1]
    C2985628
    Footer module
    Description

    Footer module

    Comment
    Description

    Comment

    Data type

    text

    Alias
    UMLS CUI [1]
    C0947611
    Date of processing
    Description

    Date of processing

    Data type

    date

    Alias
    UMLS CUI [1]
    C1709694
    Signature clinical investigator
    Description

    Signature clinical investigator

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0008961
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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
    Comorbidity
    Comorbidity number
    Item
    Comorbidity number
    integer
    C0009488 (UMLS CUI [1,1])
    C0750480 (UMLS CUI [1,2])
    Comorbidity description
    Item
    Comorbidity description
    text
    C0678257 (UMLS CUI [1,1])
    C0009488 (UMLS CUI [1,2])
    Begin
    Item
    Begin
    date
    C0808070 (UMLS CUI [1])
    End
    Item
    End
    date
    C0806020 (UMLS CUI [1])
    Ongoing
    Item
    Ongoing
    integer
    C0549178 (UMLS CUI [1])
    Therapy
    Item
    Therapy
    integer
    C0087111 (UMLS CUI [1])
    Therapy begin
    Item
    Therapy begin
    date
    C0087111 (UMLS CUI [1,1])
    C0439659 (UMLS CUI [1,2])
    Therapy end
    Item
    Therapy end
    integer
    C0087111 (UMLS CUI [1,1])
    C0444930 (UMLS CUI [1,2])
    Therapy ongoing
    Item
    Therapy ongoing
    integer
    C0549178 (UMLS CUI [1,1])
    C0039798 (UMLS CUI [1,2])
    Item Group
    Discontinuation
    C0457454 (UMLS CUI-1)
    Death date
    Item
    Death date
    date
    C1148348 (UMLS CUI [1])
    Discontinuation date
    Item
    Discontinuation date
    date
    C1444662 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Item
    Time of premature discontinuation
    integer
    C0457454 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])
    Time of premature discontinuation
    Code List
    Time of premature discontinuation
    CL Item
    Prephase (1)
    CL Item
    Cycle (2)
    C1302181 (UMLS CUI-1)
    CL Item
    Arm A, cycle (3)
    C1522541 (UMLS CUI-1)
    CL Item
    Arm B, cycle (4)
    C1522541 (UMLS CUI-1)
    CL Item
    DHAP, cycle (5)
    C0057634 (UMLS CUI-1)
    CL Item
    ESHAP, cycle (6)
    C0285858 (UMLS CUI-1)
    CL Item
    Follow-up (7)
    C1522577 (UMLS CUI-1)
    CL Item
    BEAM-R, cycle (8)
    Item
    Reason for premature discontinuation of trial participation
    integer
    C0457454 (UMLS CUI [1,1])
    C0392360 (UMLS CUI [1,2])
    Reason for premature discontinuation of trial participation
    Code List
    Reason for premature discontinuation of trial participation
    CL Item
    unknown (1)
    C0439673 (UMLS CUI-1)
    CL Item
    death (2)
    C0011065 (UMLS CUI-1)
    CL Item
    Lymphoma aftermath (3)
    C0024299 (UMLS CUI-1)
    CL Item
    disease progression  (4)
    C0242656 (UMLS CUI-1)
    CL Item
    toxicity (5)
    C0013221 (UMLS CUI-1)
    CL Item
    protocol violation (6)
    C1709750 (UMLS CUI-1)
    CL Item
    non-compliance (7)
    C0457432 (UMLS CUI-1)
    CL Item
    lost to follow-up (8)
    C1302313 (UMLS CUI-1)
    CL Item
    patient wish (9)
    C0747309 (UMLS CUI-1)
    CL Item
    Physician Decision (10)
    C1709536 (UMLS CUI-1)
    Item Group
    Adverse event
    C0877248 (UMLS CUI-1)
    Adverse event number
    Item
    Adverse event number
    integer
    C0877248 (UMLS CUI [1,1])
    C0237753 (UMLS CUI [1,2])
    Begin
    Item
    Begin
    date
    C0808070 (UMLS CUI [1])
    End
    Item
    End
    date
    C0806020 (UMLS CUI [1])
    Adverse event
    Item
    Adverse event
    text
    C0877248 (UMLS CUI [1])
    Item
    Adverse event frequency
    integer
    C0877248 (UMLS CUI [1,1])
    C0439603 (UMLS CUI [1,2])
    Adverse event frequency
    Code List
    Adverse event frequency
    CL Item
    Once (1)
    CL Item
    Twice (2)
    CL Item
    Ongoing (3)
    Item
    Adverse Event: Severity
    integer
    C1710066 (UMLS CUI [1])
    Adverse Event: Severity
    Code List
    Adverse Event: Severity
    CL Item
    Mild (Mild)
    C2945599 (UMLS CUI-1)
    CL Item
    Moderate (Moderate)
    C0205081 (UMLS CUI-1)
    CL Item
    Severe (Severe)
    C0205082 (UMLS CUI-1)
    CL Item
    Life threatening (4)
    C2826244 (UMLS CUI-1)
    CL Item
    Death (5)
    C0011065 (UMLS CUI-1)
    Item
    Adverse Event Action Code
    integer
    C0877248 (UMLS CUI [1,1])
    C0441472 (UMLS CUI [1,2])
    C0805701 (UMLS CUI [1,3])
    Adverse Event Action Code
    Code List
    Adverse Event Action Code
    CL Item
    Agent Withdrawn (1)
    C2349954 (UMLS CUI-1)
    CL Item
    Agent Dose Reduced (2)
    C0441610 (UMLS CUI-1)
    CL Item
    Agent Dose Increased (3)
    C0442805 (UMLS CUI-1)
    CL Item
    Agent Dose Not Changed (4)
    C0443172 (UMLS CUI-1)
    CL Item
    Unknown (5)
    C0439673 (UMLS CUI-1)
    CL Item
    Not Applicable (6)
    C1272460 (UMLS CUI-1)
    Item
    Correlation with trial procedure
    integer
    C1707520 (UMLS CUI [1])
    Correlation with trial procedure
    Code List
    Correlation with trial procedure
    CL Item
    definite (1)
    CL Item
    probable (2)
    CL Item
    possible (3)
    CL Item
    not likely (4)
    CL Item
    no correlation (5)
    CL Item
    can not be assessed (6)
    Item
    Result of adverse event
    integer
    C2985628 (UMLS CUI [1])
    Result of adverse event
    Code List
    Result of adverse event
    CL Item
    Patient restored (1)
    C0846605 (UMLS CUI-1)
    CL Item
    Ongoing (2)
    C0549178 (UMLS CUI-1)
    CL Item
    permanent damage (3)
    C3640792 (UMLS CUI-1)
    CL Item
    malformation (4)
    C0302142 (UMLS CUI-1)
    CL Item
    death (5)
    C0011065 (UMLS CUI-1)
    CL Item
    unknown (6)
    C0439673 (UMLS CUI-1)
    Item Group
    Footer module
    Comment
    Item
    Comment
    text
    C0947611 (UMLS CUI [1])
    Date of processing
    Item
    Date of processing
    date
    C1709694 (UMLS CUI [1])
    Signature clinical investigator
    Item
    Signature clinical investigator
    boolean
    C0008961 (UMLS CUI [1])
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