ID

16268

Description

NCT02669589 EudraCT-Nr. 2014-004854-33 REGIONAL CITRATE VERSUS SYSTEMIC HEPARIN ANTICOAGULATION FOR CONTINUOUS RENAL REPLACEMENT THERAPY IN CRITICALLY ILL PATIENTS WITH ACUTE KIDNEY INJURY Study Chair: Alexander Zarbock, MD University Hospital Muenster

Keywords

  1. 7/8/16 7/8/16 -
Uploaded on

July 8, 2016

DOI

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License

Creative Commons BY-NC-ND 3.0

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    Pre-Screening Log RICH study NCT02669589

    Pre-Screening Log RICH study NCT02669589

    Patient Information
    Description

    Patient Information

    Alias
    UMLS CUI-1
    C1955348
    ID of Center
    Description

    Center ID

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0600091
    UMLS CUI [1,2]
    C0019994
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI-1
    C1512693
    Screening Date:
    Description

    Screening Date

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C0220908
    Age of Patient:
    Description

    Age

    Data type

    float

    Measurement units
    • years
    Alias
    UMLS CUI [1]
    C0001779
    years
    Patient's gender:
    Description

    Gender

    Data type

    text

    Alias
    UMLS CUI [1]
    C0079399
    Oliguria?
    Description

    Oliguria

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0028961
    Cardiovascular Score ≥3? as soon as dose of epinephrine or norephrine is necessary: group SOFA 3-4
    Description

    Cardiovascular Score

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0007226
    UMLS CUI [1,2]
    C0449820
    Reason for Exclusion
    Description

    Reason for Exclusion

    Alias
    UMLS CUI-1
    C0392360
    UMLS CUI-2
    C0680251
    Specify which incusion or exclusion criteria are disobeyed: (if more than 3 criteria, chose the 3 most import ones)
    Description

    Inclusion or exclusion criteria

    Data type

    text

    Alias
    UMLS CUI [1]
    C1512693
    UMLS CUI [2]
    C0680251
    Other reason?
    Description

    Other reason

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C3840932
    If "other reason", specify:
    Description

    Other reason specification

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C3840932
    UMLS CUI [1,2]
    C2348235

    Similar models

    Pre-Screening Log RICH study NCT02669589

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Patient Information
    C1955348 (UMLS CUI-1)
    Center ID
    Item
    ID of Center
    text
    C0600091 (UMLS CUI [1,1])
    C0019994 (UMLS CUI [1,2])
    Item Group
    Inclusion Criteria
    C1512693 (UMLS CUI-1)
    Screening Date
    Item
    Screening Date:
    date
    C0011008 (UMLS CUI [1,1])
    C0220908 (UMLS CUI [1,2])
    Age
    Item
    Age of Patient:
    float
    C0001779 (UMLS CUI [1])
    Item
    Patient's gender:
    text
    C0079399 (UMLS CUI [1])
    Code List
    Patient's gender:
    CL Item
    male (male)
    CL Item
    female (female)
    Oliguria
    Item
    Oliguria?
    boolean
    C0028961 (UMLS CUI [1])
    Cardiovascular Score
    Item
    Cardiovascular Score ≥3? as soon as dose of epinephrine or norephrine is necessary: group SOFA 3-4
    boolean
    C0007226 (UMLS CUI [1,1])
    C0449820 (UMLS CUI [1,2])
    Item Group
    Reason for Exclusion
    C0392360 (UMLS CUI-1)
    C0680251 (UMLS CUI-2)
    Item
    Specify which incusion or exclusion criteria are disobeyed: (if more than 3 criteria, chose the 3 most import ones)
    text
    C1512693 (UMLS CUI [1])
    C0680251 (UMLS CUI [2])
    Code List
    Specify which incusion or exclusion criteria are disobeyed: (if more than 3 criteria, chose the 3 most import ones)
    CL Item
    planned unlimited intensive care for at least 3 days (98)
    CL Item
    severe sepsis/septic shock OR high catecholamine use OR refractory fluid overload: imaging/worsening of lung oedema (99)
    CL Item
    Patient with high bleeding risk (01)
    CL Item
    haemorrhagic diathesis (02)
    CL Item
    Chronic Kidney Disease (KDOQI IV without dialysis dependency) (03)
    CL Item
    after Akute Kidney Injury (within the last 90 days) (04)
    CL Item
    Chronic Kideny Disease with dialysis dependency (05)
    CL Item
    Systemic Anticoagulation (06)
    CL Item
    Allergic Reaction to anticoagulation agent or ingredients, HIT (07)
    CL Item
    Akute Kidney Injury (by occlusion or surgical lesion of A. renalis) (08)
    CL Item
    Akute Kidney Injury (by (Glomerulo-)neprhitis, interstitial nephritis, vaskulitis, postrenal obstruction) (09)
    CL Item
    patient with DNR-Order (10)
    CL Item
    Hemolytic-uremic syndroLactic acidosisenic purpura (11)
    CL Item
    long lasting and severe lactic acidosis in context with acute liver failure and/ or shock (12)
    CL Item
    condition after renal transplantation within the last 12 months (13)
    CL Item
    pregnancy or lactating (14)
    CL Item
    abortus imminens (15)
    CL Item
    no free dialysis machines availabe (16)
    CL Item
    participation in other interventional trials within the last 3 months (17)
    CL Item
    patients who have personal relation to one of the people who supervises the trial (18)
    CL Item
    people who are in an institution due to court order or administrative order (19)
    Other reason
    Item
    Other reason?
    boolean
    C3840932 (UMLS CUI [1])
    Other reason specification
    Item
    If "other reason", specify:
    text
    C3840932 (UMLS CUI [1,1])
    C2348235 (UMLS CUI [1,2])

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