0 Ratings

ID

12954

Description

Access II - Trial of Warfarin to Prevent Malfunction of Haemodialysis Catheters; ODM derived from: https://clinicaltrials.gov/show/NCT00157651

Link

https://clinicaltrials.gov/show/NCT00157651

Keywords

  1. 1/7/16 1/7/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

January 7, 2016

DOI

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License

Creative Commons BY-NC 3.0

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    Eligibility End Stage Renal Disease NCT00157651

    Eligibility End Stage Renal Disease NCT00157651

    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    newly placed double-lumen hemodialysis catheter
    Description

    newly placed double-lumen hemodialysis catheter

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0019004
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    major bleed within last 3 months
    Description

    major bleeding

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0019080
    platelet count less than 50 x 10 9/l or current coagulopathy (most recent inr > 1.5, not due to warfarin)
    Description

    platelet count or coagulopathy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0005821
    UMLS CUI [2]
    C0005779
    active peptic ulcer disease
    Description

    peptic ulcer disease

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0030920
    anticipated need for invasive intervention within next 2 weeks
    Description

    invasive intervention

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0543467
    taking warfarin for an indication other than access prophylaxis
    Description

    warfarin

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0043031
    allergic to, or intolerant of, warfarin
    Description

    allergic to, or intolerant of, warfarin

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0020517
    UMLS CUI [1,2]
    C0043031
    pregnant
    Description

    pregnant

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    woman of child-bearing age who has not agreed to use an adequate method of birth control for the duration of the study
    Description

    woman of child-bearing age who has not agreed to use an adequate method of birth control for the duration of the study

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0009871
    catheter likely needed for 2 weeks or less
    Description

    catheter likely needed for 2 weeks or less

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0007430
    patient previously took part in the study
    Description

    patient previously took part in the study

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    patient has known aortic aneurysm of 6cm or greater
    Description

    aortic aneurysm

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0003486
    patients nephrologist has refused consent
    Description

    patients nephrologist has refused consent

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    patient has refused consent
    Description

    patient has refused consent

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0021430

    Similar models

    Eligibility End Stage Renal Disease NCT00157651

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    C1512693 (UMLS CUI)
    newly placed double-lumen hemodialysis catheter
    Item
    newly placed double-lumen hemodialysis catheter
    boolean
    C0019004 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    major bleeding
    Item
    major bleed within last 3 months
    boolean
    C0019080 (UMLS CUI [1])
    platelet count or coagulopathy
    Item
    platelet count less than 50 x 10 9/l or current coagulopathy (most recent inr > 1.5, not due to warfarin)
    boolean
    C0005821 (UMLS CUI [1])
    C0005779 (UMLS CUI [2])
    peptic ulcer disease
    Item
    active peptic ulcer disease
    boolean
    C0030920 (UMLS CUI [1])
    invasive intervention
    Item
    anticipated need for invasive intervention within next 2 weeks
    boolean
    C0543467 (UMLS CUI [1])
    warfarin
    Item
    taking warfarin for an indication other than access prophylaxis
    boolean
    C0043031 (UMLS CUI [1])
    allergic to, or intolerant of, warfarin
    Item
    allergic to, or intolerant of, warfarin
    boolean
    C0020517 (UMLS CUI [1,1])
    C0043031 (UMLS CUI [1,2])
    pregnant
    Item
    pregnant
    boolean
    C0032961 (UMLS CUI [1])
    woman of child-bearing age who has not agreed to use an adequate method of birth control for the duration of the study
    Item
    woman of child-bearing age who has not agreed to use an adequate method of birth control for the duration of the study
    boolean
    C0009871 (UMLS CUI [1])
    catheter likely needed for 2 weeks or less
    Item
    catheter likely needed for 2 weeks or less
    boolean
    C0007430 (UMLS CUI [1])
    patient previously took part in the study
    Item
    patient previously took part in the study
    boolean
    C2348568 (UMLS CUI [1])
    aortic aneurysm
    Item
    patient has known aortic aneurysm of 6cm or greater
    boolean
    C0003486 (UMLS CUI [1])
    patients nephrologist has refused consent
    Item
    patients nephrologist has refused consent
    boolean
    C0021430 (UMLS CUI [1])
    patient has refused consent
    Item
    patient has refused consent
    boolean
    C0021430 (UMLS CUI [1])

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