0 Ratings
ID

40455

Description

The Long-term Prognosis of Moderate to Severe Bronchial Hyperresponsiveness (BHR) in Asthmatic Preschool Children; ODM derived from: https://clinicaltrials.gov/show/NCT01144910

Link

https://clinicaltrials.gov/show/NCT01144910

Keywords

Versions (1)
  1. 4/23/20 4/23/20 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

April 23, 2020

DOI

To request one please log in.

License

Creative Commons BY 4.0
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.

Back to model comments
Itemgroup comments for :

Item comments for :

  • Newest
  • Oldest
  • Popular
  • Newest
    • Newest
    • Oldest
    • Popular

    No comments

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

    Eligibility Intrinsic Asthma NCT01144910

    English

    Eligibility Intrinsic Asthma NCT01144910

    1 forms  
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    informed consent
    Description

    Informed Consent

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    age 3 to 6 years
    Description

    Age

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    diagnosis asthma
    Description

    Asthma

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0004096
    pulmonary function: fev1 (% pred.)≥ 70%
    Description

    Pulmonary function | Percent predicted FEV1

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0231921
    UMLS CUI [2]
    C0730561
    ability to carry out 2 reproducible flow volume loops
    Description

    Ability Flow volume loop Quantity

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0085732
    UMLS CUI [1,2]
    C0428734
    UMLS CUI [1,3]
    C1265611
    moderate to severe bhr (pd20 fev1 ≤ 0,3 mg methacholine)
    Description

    Bronchial Hyperreactivity Moderate | Bronchial Hyperreactivity Severe | FEV1 Methacholine

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0085129
    UMLS CUI [1,2]
    C0205081
    UMLS CUI [2,1]
    C0085129
    UMLS CUI [2,2]
    C0205082
    UMLS CUI [3,1]
    C0849974
    UMLS CUI [3,2]
    C0600370
    more than 4 weeks interval since last infection
    Description

    Interval Since Communicable Disease

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1272706
    UMLS CUI [1,2]
    C1711239
    UMLS CUI [1,3]
    C0009450
    8 hours washout period of short acting beta agonist
    Description

    Washout Period Adrenergic beta-Agonists Active short-term

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1710661
    UMLS CUI [1,2]
    C0001644
    UMLS CUI [1,3]
    C0205177
    UMLS CUI [1,4]
    C0443303
    1 week washout period of ipratropium bromide
    Description

    Washout Period Ipratropium Bromide

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1710661
    UMLS CUI [1,2]
    C0700580
    1 week washout period of long acting beta agonist
    Description

    Washout Period Adrenergic beta-Agonists Active Long-term

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1710661
    UMLS CUI [1,2]
    C0001644
    UMLS CUI [1,3]
    C0205177
    UMLS CUI [1,4]
    C0443252
    4 weeks washout period of systemic corticosteroids
    Description

    Washout Period CORTICOSTEROIDS FOR SYSTEMIC USE

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1710661
    UMLS CUI [1,2]
    C3653708
    4 weeks washout period of leukotriene antagonists
    Description

    Washout Period Leukotriene Antagonists

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1710661
    UMLS CUI [1,2]
    C0595726
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    age < 3 and > 6 years
    Description

    Age

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    pulmonary function test: fev1 (% pred.) < 70%
    Description

    Pulmonary function test | Percent predicted FEV1

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0024119
    UMLS CUI [2]
    C0730561
    others chronic diseases or infections (e.g., hiv, tuberculosis, malignancy)
    Description

    Chronic disease | Chronic infectious disease | HIV Infection | Tuberculosis | Malignant Neoplasms

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0008679
    UMLS CUI [2]
    C0151317
    UMLS CUI [3]
    C0019693
    UMLS CUI [4]
    C0041296
    UMLS CUI [5]
    C0006826
    incapability to perform spirometry
    Description

    Spirometry Perform Unable

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0037981
    UMLS CUI [1,2]
    C0884358
    UMLS CUI [1,3]
    C1299582
    current participation in another clinical trial
    Description

    Study Subject Participation Status | Clinical Trial

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    UMLS CUI [2]
    C0008976
    Back to the top of the page

    Similar models

    Eligibility Intrinsic Asthma NCT01144910

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Informed Consent
    Item
    informed consent
    boolean
    C0021430 (UMLS CUI [1])
    Age
    Item
    age 3 to 6 years
    boolean
    C0001779 (UMLS CUI [1])
    Asthma
    Item
    diagnosis asthma
    boolean
    C0004096 (UMLS CUI [1])
    Pulmonary function | Percent predicted FEV1
    Item
    pulmonary function: fev1 (% pred.)≥ 70%
    boolean
    C0231921 (UMLS CUI [1])
    C0730561 (UMLS CUI [2])
    Ability Flow volume loop Quantity
    Item
    ability to carry out 2 reproducible flow volume loops
    boolean
    C0085732 (UMLS CUI [1,1])
    C0428734 (UMLS CUI [1,2])
    C1265611 (UMLS CUI [1,3])
    Bronchial Hyperreactivity Moderate | Bronchial Hyperreactivity Severe | FEV1 Methacholine
    Item
    moderate to severe bhr (pd20 fev1 ≤ 0,3 mg methacholine)
    boolean
    C0085129 (UMLS CUI [1,1])
    C0205081 (UMLS CUI [1,2])
    C0085129 (UMLS CUI [2,1])
    C0205082 (UMLS CUI [2,2])
    C0849974 (UMLS CUI [3,1])
    C0600370 (UMLS CUI [3,2])
    Interval Since Communicable Disease
    Item
    more than 4 weeks interval since last infection
    boolean
    C1272706 (UMLS CUI [1,1])
    C1711239 (UMLS CUI [1,2])
    C0009450 (UMLS CUI [1,3])
    Washout Period Adrenergic beta-Agonists Active short-term
    Item
    8 hours washout period of short acting beta agonist
    boolean
    C1710661 (UMLS CUI [1,1])
    C0001644 (UMLS CUI [1,2])
    C0205177 (UMLS CUI [1,3])
    C0443303 (UMLS CUI [1,4])
    Washout Period Ipratropium Bromide
    Item
    1 week washout period of ipratropium bromide
    boolean
    C1710661 (UMLS CUI [1,1])
    C0700580 (UMLS CUI [1,2])
    Washout Period Adrenergic beta-Agonists Active Long-term
    Item
    1 week washout period of long acting beta agonist
    boolean
    C1710661 (UMLS CUI [1,1])
    C0001644 (UMLS CUI [1,2])
    C0205177 (UMLS CUI [1,3])
    C0443252 (UMLS CUI [1,4])
    Washout Period CORTICOSTEROIDS FOR SYSTEMIC USE
    Item
    4 weeks washout period of systemic corticosteroids
    boolean
    C1710661 (UMLS CUI [1,1])
    C3653708 (UMLS CUI [1,2])
    Washout Period Leukotriene Antagonists
    Item
    4 weeks washout period of leukotriene antagonists
    boolean
    C1710661 (UMLS CUI [1,1])
    C0595726 (UMLS CUI [1,2])
    Item Group
    C0680251 (UMLS CUI)
    Age
    Item
    age < 3 and > 6 years
    boolean
    C0001779 (UMLS CUI [1])
    Pulmonary function test | Percent predicted FEV1
    Item
    pulmonary function test: fev1 (% pred.) < 70%
    boolean
    C0024119 (UMLS CUI [1])
    C0730561 (UMLS CUI [2])
    Chronic disease | Chronic infectious disease | HIV Infection | Tuberculosis | Malignant Neoplasms
    Item
    others chronic diseases or infections (e.g., hiv, tuberculosis, malignancy)
    boolean
    C0008679 (UMLS CUI [1])
    C0151317 (UMLS CUI [2])
    C0019693 (UMLS CUI [3])
    C0041296 (UMLS CUI [4])
    C0006826 (UMLS CUI [5])
    Spirometry Perform Unable
    Item
    incapability to perform spirometry
    boolean
    C0037981 (UMLS CUI [1,1])
    C0884358 (UMLS CUI [1,2])
    C1299582 (UMLS CUI [1,3])
    Study Subject Participation Status | Clinical Trial
    Item
    current participation in another clinical trial
    boolean
    C2348568 (UMLS CUI [1])
    C0008976 (UMLS CUI [2])
    Back to the top of the page 

    Help

    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