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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

Lien

https://clinicaltrials.gov/show/NCT01144910

Mots-clés

Versions (1)
  1. 23/04/2020 23/04/2020 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

23 avril 2020

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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    Eligibility Intrinsic Asthma NCT01144910

    Anglais

    Eligibility Intrinsic Asthma NCT01144910

    1 Formulaires  
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    informed consent
    Description

    Informed Consent

    Type de données

    boolean

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

    Age

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    diagnosis asthma
    Description

    Asthma

    Type de données

    boolean

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

    Pulmonary function | Percent predicted FEV1

    Type de données

    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

    Type de données

    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

    Type de données

    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

    Type de données

    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

    Type de données

    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

    Type de données

    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

    Type de données

    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

    Type de données

    boolean

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

    Washout Period Leukotriene Antagonists

    Type de données

    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

    Type de données

    boolean

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

    Pulmonary function test | Percent predicted FEV1

    Type de données

    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

    Type de données

    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

    Type de données

    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

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    UMLS CUI [2]
    C0008976
    Retour au début de la page

    Similar models

    Eligibility Intrinsic Asthma NCT01144910

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    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])
    Retour au début de la page 

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