0 Ratings
ID

41590

Description

The TRUST Study - Depression Substudy; ODM derived from: https://clinicaltrials.gov/show/NCT01853579

Link

https://clinicaltrials.gov/show/NCT01853579

Keywords

Versions (1)
  1. 11/18/20 11/18/20 -
Copyright Holder

see on clinicaltrials.gov

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November 18, 2020

DOI

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License

Creative Commons BY 4.0
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    Eligibility Subclinical Hypothyroidism NCT01853579

    English

    Eligibility Subclinical Hypothyroidism NCT01853579

    1 forms  
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    community-dwelling patients aged >= 65 years with subclinical hypothyroidism
    Description

    community-dwelling patients aged >= 65 years with subclinical hypothyroidism

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C4045975
    UMLS CUI [2]
    C0001779
    UMLS CUI [3,1]
    C0020676
    UMLS CUI [3,2]
    C0205211
    written informed consent
    Description

    informed consent

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    subjects currently on levothyroxine or antithyroid drugs, amiodarone or lithium
    Description

    currently on levothyroxine or antithyroid drugs, amiodarone or lithium

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C2827774
    UMLS CUI [1,2]
    C0040165
    UMLS CUI [2,1]
    C2827774
    UMLS CUI [2,2]
    C0040125
    UMLS CUI [3,1]
    C2827774
    UMLS CUI [3,2]
    C0002598
    UMLS CUI [4,1]
    C2827774
    UMLS CUI [4,2]
    C0023870
    recent thyroid surgery or radio-iodine (within 12 months)
    Description

    recent thyroid surgery or radio-iodine

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0332185
    UMLS CUI [1,2]
    C0193769
    UMLS CUI [2,1]
    C0332185
    UMLS CUI [2,2]
    C2169308
    grade iv nyha heart failure
    Description

    grade iv nyha heart failure

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0018801
    UMLS CUI [1,2]
    C1275491
    prior clinical diagnosis of dementia
    Description

    prior clinical diagnosis of dementia

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0332132
    UMLS CUI [1,2]
    C0497327
    recent hospitalisation for major illness or elective surgery (within 4 weeks)
    Description

    recent hospitalisation for major illness or elective surgery

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0332185
    UMLS CUI [1,2]
    C0019993
    UMLS CUI [1,3]
    C0221423
    UMLS CUI [1,4]
    C0205164
    UMLS CUI [2,1]
    C0332185
    UMLS CUI [2,2]
    C0019993
    UMLS CUI [2,3]
    C0206058
    terminal illness
    Description

    terminal illness

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0679247
    patients with hereditary problems of galactose intolerance, the lapp lactase deficiency or glucose-galactose malabsorption
    Description

    rare hereditary problems of galactose intolerance, the lapp lactase deficiency or glucose-galactose malabsorption

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0016952
    UMLS CUI [1,2]
    C0439660
    UMLS CUI [2,1]
    C0337904
    UMLS CUI [2,2]
    C0302813
    UMLS CUI [3]
    C0268186
    subjects who are participating in ongoing rcts of therapeutic interventions (including ctimps)
    Description

    participation in ongoing rcts

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C2348568
    UMLS CUI [1,2]
    C0549178
    UMLS CUI [1,3]
    C0206035
    plan to move out of the region in which the trial is being conducted within the next 2 years (proposed minimum follow-up period)
    Description

    plan to move out of the region in which the trial is being conducted within the next 2 years

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C2699029
    UMLS CUI [1,2]
    C1301732
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    Similar models

    Eligibility Subclinical Hypothyroidism NCT01853579

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    C1512693 (UMLS CUI)
    community-dwelling patients aged >= 65 years with subclinical hypothyroidism
    Item
    community-dwelling patients aged >= 65 years with subclinical hypothyroidism
    boolean
    C4045975 (UMLS CUI [1])
    C0001779 (UMLS CUI [2])
    C0020676 (UMLS CUI [3,1])
    C0205211 (UMLS CUI [3,2])
    informed consent
    Item
    written informed consent
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    currently on levothyroxine or antithyroid drugs, amiodarone or lithium
    Item
    subjects currently on levothyroxine or antithyroid drugs, amiodarone or lithium
    boolean
    C2827774 (UMLS CUI [1,1])
    C0040165 (UMLS CUI [1,2])
    C2827774 (UMLS CUI [2,1])
    C0040125 (UMLS CUI [2,2])
    C2827774 (UMLS CUI [3,1])
    C0002598 (UMLS CUI [3,2])
    C2827774 (UMLS CUI [4,1])
    C0023870 (UMLS CUI [4,2])
    recent thyroid surgery or radio-iodine
    Item
    recent thyroid surgery or radio-iodine (within 12 months)
    boolean
    C0332185 (UMLS CUI [1,1])
    C0193769 (UMLS CUI [1,2])
    C0332185 (UMLS CUI [2,1])
    C2169308 (UMLS CUI [2,2])
    grade iv nyha heart failure
    Item
    grade iv nyha heart failure
    boolean
    C0018801 (UMLS CUI [1,1])
    C1275491 (UMLS CUI [1,2])
    prior clinical diagnosis of dementia
    Item
    prior clinical diagnosis of dementia
    boolean
    C0332132 (UMLS CUI [1,1])
    C0497327 (UMLS CUI [1,2])
    recent hospitalisation for major illness or elective surgery
    Item
    recent hospitalisation for major illness or elective surgery (within 4 weeks)
    boolean
    C0332185 (UMLS CUI [1,1])
    C0019993 (UMLS CUI [1,2])
    C0221423 (UMLS CUI [1,3])
    C0205164 (UMLS CUI [1,4])
    C0332185 (UMLS CUI [2,1])
    C0019993 (UMLS CUI [2,2])
    C0206058 (UMLS CUI [2,3])
    terminal illness
    Item
    terminal illness
    boolean
    C0679247 (UMLS CUI [1])
    rare hereditary problems of galactose intolerance, the lapp lactase deficiency or glucose-galactose malabsorption
    Item
    patients with hereditary problems of galactose intolerance, the lapp lactase deficiency or glucose-galactose malabsorption
    boolean
    C0016952 (UMLS CUI [1,1])
    C0439660 (UMLS CUI [1,2])
    C0337904 (UMLS CUI [2,1])
    C0302813 (UMLS CUI [2,2])
    C0268186 (UMLS CUI [3])
    participation in ongoing rcts
    Item
    subjects who are participating in ongoing rcts of therapeutic interventions (including ctimps)
    boolean
    C2348568 (UMLS CUI [1,1])
    C0549178 (UMLS CUI [1,2])
    C0206035 (UMLS CUI [1,3])
    plan to move out of the region in which the trial is being conducted within the next 2 years
    Item
    plan to move out of the region in which the trial is being conducted within the next 2 years (proposed minimum follow-up period)
    boolean
    C2699029 (UMLS CUI [1,1])
    C1301732 (UMLS CUI [1,2])
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