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ID

14149

Beschrijving

Asthma Biomarkers for Predicting Response to Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT01973751

Link

https://clinicaltrials.gov/show/NCT01973751

Trefwoorden

Versies (1)
  1. 01-04-16 01-04-16 -
Geüploaded op

1 april 2016

DOI

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Licentie

Creative Commons BY 4.0
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    Eligibility Asthma NCT01973751

    Engels

    Eligibility Asthma NCT01973751

    1 Formulieren  
    1. StudyEvent: Eligibility
      1. Eligibility Asthma NCT01973751
    Criteria
    Beschrijving

    Criteria

    Inclusion Criteria
    Beschrijving

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    male and female subjects between the ages of 18 and 70 years
    Beschrijving

    Age | Gender

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0001779
    UMLS CUI [1,2]
    C0079399
    no respiratory symptoms
    Beschrijving

    No respiratory symptoms

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0425443
    normal spirometric value and methacholine pd20 >2.5mg
    Beschrijving

    Spirometry normal | Methacholine

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0855776
    UMLS CUI [2]
    C0600370
    group b:
    Beschrijving

    ID.4

    Datatype

    boolean

    Inclusion Criteria
    Beschrijving

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    male and female subjects between the ages of 18 and 70 years
    Beschrijving

    Age | Gender

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    UMLS CUI [2]
    C0079399
    history of asthma
    Beschrijving

    Asthma

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0004096
    no use of oral or inhaled corticosteroids for the treatment of asthma
    Beschrijving

    Therapeutic procedure | Asthma | Adrenal Cortex Hormones | inhaled steroids

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0087111
    UMLS CUI [1,2]
    C0004096
    UMLS CUI [2]
    C0001617
    UMLS CUI [3]
    C2065041
    no use of leukotriene antagonist for the treatment of asthma
    Beschrijving

    Therapeutic procedure | Asthma | Leukotriene Antagonists

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0087111
    UMLS CUI [1,2]
    C0004096
    UMLS CUI [2]
    C0595726
    hyperreactivity to methacholine (pd20 fev1 methacholine < 2.5 mg) and/or ≥12% increase in fev1 following inhalation of 200μg salbutamol
    Beschrijving

    Pulmonary methacholine challenge test | FEV1 | Albuterol

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C1096470
    UMLS CUI [2]
    C0748133
    UMLS CUI [3]
    C0001927
    asthma symptoms of episodic cough, wheeze and/or breathlessness
    Beschrijving

    Asthma symptoms | Coughing | Rhonchi | Dyspnea

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0004096
    UMLS CUI [1,2]
    C1457887
    UMLS CUI [2]
    C0010200
    UMLS CUI [3]
    C0035508
    UMLS CUI [4]
    C0013404
    Exclusion Criteria
    Beschrijving

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    current or former smokers
    Beschrijving

    Current Smoker | Former smoker

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C3241966
    UMLS CUI [2]
    C0337671
    pregnant women
    Beschrijving

    Pregnancy

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    subjects with a history of lung disease other than asthma
    Beschrijving

    Lung disease

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0024115
    UMLS CUI [2]
    C0004096
    subjects with a history of a medical disease, which in the opinion of the investigator may put the subject at extra risk from study-related procedures or because the disease may influence the results of the study
    Beschrijving

    Disease | Study Subject Participation Status

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0012634
    UMLS CUI [2]
    C2348568
    Terug naar het begin van de pagina

    Similar models

    Eligibility Asthma NCT01973751

    1 Formulieren
    1. StudyEvent: Eligibility
      1. Eligibility Asthma NCT01973751
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Item Group
    C1512693 (UMLS CUI)
    Age | Gender
    Item
    male and female subjects between the ages of 18 and 70 years
    boolean
    C0001779 (UMLS CUI [1,1])
    C0079399 (UMLS CUI [1,2])
    No respiratory symptoms
    Item
    no respiratory symptoms
    boolean
    C0425443 (UMLS CUI [1])
    Spirometry normal | Methacholine
    Item
    normal spirometric value and methacholine pd20 >2.5mg
    boolean
    C0855776 (UMLS CUI [1])
    C0600370 (UMLS CUI [2])
    ID.4
    Item
    group b:
    boolean
    Item Group
    C1512693 (UMLS CUI)
    Age | Gender
    Item
    male and female subjects between the ages of 18 and 70 years
    boolean
    C0001779 (UMLS CUI [1])
    C0079399 (UMLS CUI [2])
    Asthma
    Item
    history of asthma
    boolean
    C0004096 (UMLS CUI [1])
    Therapeutic procedure | Asthma | Adrenal Cortex Hormones | inhaled steroids
    Item
    no use of oral or inhaled corticosteroids for the treatment of asthma
    boolean
    C0087111 (UMLS CUI [1,1])
    C0004096 (UMLS CUI [1,2])
    C0001617 (UMLS CUI [2])
    C2065041 (UMLS CUI [3])
    Therapeutic procedure | Asthma | Leukotriene Antagonists
    Item
    no use of leukotriene antagonist for the treatment of asthma
    boolean
    C0087111 (UMLS CUI [1,1])
    C0004096 (UMLS CUI [1,2])
    C0595726 (UMLS CUI [2])
    Pulmonary methacholine challenge test | FEV1 | Albuterol
    Item
    hyperreactivity to methacholine (pd20 fev1 methacholine < 2.5 mg) and/or ≥12% increase in fev1 following inhalation of 200μg salbutamol
    boolean
    C1096470 (UMLS CUI [1])
    C0748133 (UMLS CUI [2])
    C0001927 (UMLS CUI [3])
    Asthma symptoms | Coughing | Rhonchi | Dyspnea
    Item
    asthma symptoms of episodic cough, wheeze and/or breathlessness
    boolean
    C0004096 (UMLS CUI [1,1])
    C1457887 (UMLS CUI [1,2])
    C0010200 (UMLS CUI [2])
    C0035508 (UMLS CUI [3])
    C0013404 (UMLS CUI [4])
    Item Group
    C0680251 (UMLS CUI)
    Current Smoker | Former smoker
    Item
    current or former smokers
    boolean
    C3241966 (UMLS CUI [1])
    C0337671 (UMLS CUI [2])
    Pregnancy
    Item
    pregnant women
    boolean
    C0032961 (UMLS CUI [1])
    Lung disease
    Item
    subjects with a history of lung disease other than asthma
    boolean
    C0024115 (UMLS CUI [1])
    C0004096 (UMLS CUI [2])
    Disease | Study Subject Participation Status
    Item
    subjects with a history of a medical disease, which in the opinion of the investigator may put the subject at extra risk from study-related procedures or because the disease may influence the results of the study
    boolean
    C0012634 (UMLS CUI [1])
    C2348568 (UMLS CUI [2])
    Terug naar het begin van de pagina 

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