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ID

43525

Description

A Study To Investigate The Effect Of Inhaled Fluticasone Propionate On The Bronchial Responsiveness To Leukotriene D4 In Asthmatics Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00453778

Link

https://clinicaltrials.gov/show/NCT00453778

Keywords

  1. 4/12/16 4/12/16 -
  2. 9/20/21 9/20/21 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

September 20, 2021

DOI

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License

Creative Commons BY-NC 3.0

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    Eligibility Asthma NCT00453778

    Eligibility Asthma NCT00453778

    1. StudyEvent: Eligibility
      1. Eligibility Asthma NCT00453778
    Criteria
    Description

    Criteria

    diagnosed history of asthma
    Description

    history of asthma

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0262926
    UMLS CUI [1,2]
    C0004096
    non smoker last two years
    Description

    non-smoker

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0337672
    UMLS CUI [1,2]
    C0040223
    < 5 pack years
    Description

    pack years

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1277691
    fev1 >70% of predicted
    Description

    fev1

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0748133
    mild and stable asthma
    Description

    mild and stable asthma

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0741266
    UMLS CUI [1,2]
    C2945599
    only using short acting b2-agonist as rescue for the last 4 weeks
    Description

    short acting b2-agonist

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1373132
    have a history of atopy.
    Description

    atopy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0392707
    exclusion:
    Description

    exclusion

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2828389
    any significant respiratory disease, other than asthma
    Description

    respiratory disease

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0035204
    subjects with seasonal asthma may not be included if they are in their season
    Description

    seasonal asthma

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2919352
    use of oral or inhaled glucocorticosteroid for the last 3 months and long-acting or oral b2-agonists, anticholinergic bronchodilators, cromones, antihistamines, theophyllines and antileukotrienes within two weeks
    Description

    corticosteroids, b2-agonists, anticholinergic bronchodilators, cromones, antihistamines, theophyllines, antileukotrienes

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0001617
    UMLS CUI [2]
    C1373132
    UMLS CUI [3]
    C0039771
    UMLS CUI [4]
    C0354764
    UMLS CUI [5]
    C0019590
    UMLS CUI [6]
    C0595726
    upper or lower rti within 6 weeks
    Description

    respiratory tract infection

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0035243
    UMLS CUI [1,2]
    C0040223
    evidence of any disease that in the investigators mind would affect the results of the study
    Description

    comorbidity limiting study protocol

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1321605
    UMLS CUI [1,2]
    C0439801
    UMLS CUI [1,3]
    C0009488
    participating in another study within 4 weeks
    Description

    participating in another study within 4 weeks

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    females who are pregnant, intend to be or who are lactating
    Description

    pregnancy, lactation, intention to become pregnant

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2,1]
    C0032961
    UMLS CUI [2,2]
    C1283828
    UMLS CUI [3]
    C0006147
    methacholine pd20 > 454mcg
    Description

    methacholine pd20

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0600370
    negative scin prick test
    Description

    skin prick test

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0430561

    Similar models

    Eligibility Asthma NCT00453778

    1. StudyEvent: Eligibility
      1. Eligibility Asthma NCT00453778
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    history of asthma
    Item
    diagnosed history of asthma
    boolean
    C0262926 (UMLS CUI [1,1])
    C0004096 (UMLS CUI [1,2])
    non-smoker
    Item
    non smoker last two years
    boolean
    C0337672 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])
    pack years
    Item
    < 5 pack years
    boolean
    C1277691 (UMLS CUI [1])
    fev1
    Item
    fev1 >70% of predicted
    boolean
    C0748133 (UMLS CUI [1])
    mild and stable asthma
    Item
    mild and stable asthma
    boolean
    C0741266 (UMLS CUI [1,1])
    C2945599 (UMLS CUI [1,2])
    short acting b2-agonist
    Item
    only using short acting b2-agonist as rescue for the last 4 weeks
    boolean
    C1373132 (UMLS CUI [1])
    atopy
    Item
    have a history of atopy.
    boolean
    C0392707 (UMLS CUI [1])
    exclusion
    Item
    exclusion:
    boolean
    C2828389 (UMLS CUI [1])
    respiratory disease
    Item
    any significant respiratory disease, other than asthma
    boolean
    C0035204 (UMLS CUI [1])
    seasonal asthma
    Item
    subjects with seasonal asthma may not be included if they are in their season
    boolean
    C2919352 (UMLS CUI [1])
    corticosteroids, b2-agonists, anticholinergic bronchodilators, cromones, antihistamines, theophyllines, antileukotrienes
    Item
    use of oral or inhaled glucocorticosteroid for the last 3 months and long-acting or oral b2-agonists, anticholinergic bronchodilators, cromones, antihistamines, theophyllines and antileukotrienes within two weeks
    boolean
    C0001617 (UMLS CUI [1])
    C1373132 (UMLS CUI [2])
    C0039771 (UMLS CUI [3])
    C0354764 (UMLS CUI [4])
    C0019590 (UMLS CUI [5])
    C0595726 (UMLS CUI [6])
    respiratory tract infection
    Item
    upper or lower rti within 6 weeks
    boolean
    C0035243 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])
    comorbidity limiting study protocol
    Item
    evidence of any disease that in the investigators mind would affect the results of the study
    boolean
    C1321605 (UMLS CUI [1,1])
    C0439801 (UMLS CUI [1,2])
    C0009488 (UMLS CUI [1,3])
    participating in another study within 4 weeks
    Item
    participating in another study within 4 weeks
    boolean
    C2348568 (UMLS CUI [1])
    pregnancy, lactation, intention to become pregnant
    Item
    females who are pregnant, intend to be or who are lactating
    boolean
    C0032961 (UMLS CUI [1])
    C0032961 (UMLS CUI [2,1])
    C1283828 (UMLS CUI [2,2])
    C0006147 (UMLS CUI [3])
    methacholine pd20
    Item
    methacholine pd20 > 454mcg
    boolean
    C0600370 (UMLS CUI [1])
    skin prick test
    Item
    negative scin prick test
    boolean
    C0430561 (UMLS CUI [1])

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