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ID

14404

Descrizione

Monitoring Asthma Treatment Using Exhaled Nitric Oxide; ODM derived from: https://clinicaltrials.gov/show/NCT00562991

collegamento

https://clinicaltrials.gov/show/NCT00562991

Keywords

  1. 13/04/16 13/04/16 -
Titolare del copyright

CC BY-NC 3.0

Caricato su

13 aprile 2016

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0

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    Eligibility Asthma NCT00562991

    Eligibility Asthma NCT00562991

    1. StudyEvent: Eligibility
      1. Eligibility Asthma NCT00562991
    Inclusion Criteria
    Descrizione

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693 (Inclusion)
    male or female children, aged 6-14 years
    Descrizione

    age

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0001779 (Age)
    SNOMED
    424144002
    LOINC
    LP28815-6
    a documented history of asthma for a period of at least 6 months
    Descrizione

    asthma

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0004096 (Asthma)
    SNOMED
    195967001
    LOINC
    MTHU020815
    UMLS CUI [1,2]
    C0040223 (Time)
    SNOMED
    410670007
    LOINC
    LP73517-2
    mild to severe persistent asthma according to gina guidelines
    Descrizione

    mild to severe persistent asthma

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C2945599 (Mild (qualifier value))
    SNOMED
    255604002
    LOINC
    LA6752-5
    UMLS CUI [1,2]
    C0205082 (Severe (severity modifier))
    SNOMED
    24484000
    LOINC
    LA6750-9
    UMLS CUI [1,3]
    C3266628 (Persistent asthma)
    SNOMED
    5281000124103
    a documented history of allergic sensitization (positive skin prick test or specific ige
    Descrizione

    allergic sensitization

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C3662483 (Allergic sensitization)
    SNOMED
    609327009
    UMLS CUI [2]
    C0430561 (Skin prick test)
    SNOMED
    37968009
    subject's guardian/parent should be able to complete a symptom score on behalf of the subject.
    Descrizione

    subject's guardian/parent should be able to complete a symptom score on behalf of the subject

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C1321605 (Compliance behavior)
    SNOMED
    405078008
    subject's guardian/parent should be able to send a symptom score weekly by sms
    Descrizione

    subject's guardian/parent should be able to send a symptom score weekly by sms

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C1321605 (Compliance behavior)
    SNOMED
    405078008
    both parents have to give written informed consent to participate in the study
    Descrizione

    written informed consent

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0021430 (Informed Consent)
    Exclusion Criteria
    Descrizione

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251 (Exclusion Criteria)
    received any investigational study medication in the 4 weeks prior to screening visit
    Descrizione

    investigational drug

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0013230 (Investigational New Drugs)
    UMLS CUI [1,2]
    C0040223 (Time)
    SNOMED
    410670007
    LOINC
    LP73517-2
    significant comorbidity such as concurrent infection, history of prematurity, history of bronchopulmonary dysplasia, cystic fibrosis, other chronic lung diseases, and other severe chronic diseases
    Descrizione

    significant comorbidity

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0009488 (Comorbidity)
    acute asthma exacerbation within 4 weeks of screening visit
    Descrizione

    asthma exacerbation

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0349790 (Exacerbation of asthma)
    SNOMED
    281239006
    UMLS CUI [1,2]
    C0040223 (Time)
    SNOMED
    410670007
    LOINC
    LP73517-2
    hospitalization within 12 weeks of screening visit
    Descrizione

    hospitalization

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0019993 (Hospitalization)
    SNOMED
    394656005
    LOINC
    LA15417-1
    UMLS CUI [1,2]
    C0040223 (Time)
    SNOMED
    410670007
    LOINC
    LP73517-2
    systemic corticosteroids within 12 weeks of screening visit
    Descrizione

    systemic corticosteroids

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C4039704 (History of systemic steroid therapy)
    SNOMED
    134671000119104
    oral corticosteroid dependence
    Descrizione

    oral corticosteroid dependence

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1,1]
    C0001617 (Adrenal Cortex Hormones)
    SNOMED
    21568003
    LOINC
    LP20687-7
    UMLS CUI [1,2]
    C0442027 (Oral)
    SNOMED
    260548002
    LOINC
    LP32603-0
    UMLS CUI [1,3]
    C0439857 (Dependence)
    SNOMED
    103326000

    Similar models

    Eligibility Asthma NCT00562991

    1. StudyEvent: Eligibility
      1. Eligibility Asthma NCT00562991
    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    Alias
    Item Group
    C1512693 (UMLS CUI)
    age
    Item
    male or female children, aged 6-14 years
    boolean
    C0001779 (UMLS CUI [1])
    asthma
    Item
    a documented history of asthma for a period of at least 6 months
    boolean
    C0004096 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])
    mild to severe persistent asthma
    Item
    mild to severe persistent asthma according to gina guidelines
    boolean
    C2945599 (UMLS CUI [1,1])
    C0205082 (UMLS CUI [1,2])
    C3266628 (UMLS CUI [1,3])
    allergic sensitization
    Item
    a documented history of allergic sensitization (positive skin prick test or specific ige
    boolean
    C3662483 (UMLS CUI [1])
    C0430561 (UMLS CUI [2])
    subject's guardian/parent should be able to complete a symptom score on behalf of the subject
    Item
    subject's guardian/parent should be able to complete a symptom score on behalf of the subject.
    boolean
    C1321605 (UMLS CUI [1])
    subject's guardian/parent should be able to send a symptom score weekly by sms
    Item
    subject's guardian/parent should be able to send a symptom score weekly by sms
    boolean
    C1321605 (UMLS CUI [1])
    written informed consent
    Item
    both parents have to give written informed consent to participate in the study
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    investigational drug
    Item
    received any investigational study medication in the 4 weeks prior to screening visit
    boolean
    C0013230 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])
    significant comorbidity
    Item
    significant comorbidity such as concurrent infection, history of prematurity, history of bronchopulmonary dysplasia, cystic fibrosis, other chronic lung diseases, and other severe chronic diseases
    boolean
    C0009488 (UMLS CUI [1])
    asthma exacerbation
    Item
    acute asthma exacerbation within 4 weeks of screening visit
    boolean
    C0349790 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])
    hospitalization
    Item
    hospitalization within 12 weeks of screening visit
    boolean
    C0019993 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])
    systemic corticosteroids
    Item
    systemic corticosteroids within 12 weeks of screening visit
    boolean
    C4039704 (UMLS CUI [1])
    oral corticosteroid dependence
    Item
    oral corticosteroid dependence
    boolean
    C0001617 (UMLS CUI [1,1])
    C0442027 (UMLS CUI [1,2])
    C0439857 (UMLS CUI [1,3])

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