0 Avaliações

ID

14404

Descrição

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

Link

https://clinicaltrials.gov/show/NCT00562991

Palavras-chave

  1. 13/04/2016 13/04/2016 -
Titular dos direitos

CC BY-NC 3.0

Transferido a

13 de abril de 2016

DOI

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Licença

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
    Descrição

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    male or female children, aged 6-14 years
    Descrição

    age

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    a documented history of asthma for a period of at least 6 months
    Descrição

    asthma

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0004096
    UMLS CUI [1,2]
    C0040223
    mild to severe persistent asthma according to gina guidelines
    Descrição

    mild to severe persistent asthma

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C2945599
    UMLS CUI [1,2]
    C0205082
    UMLS CUI [1,3]
    C3266628
    a documented history of allergic sensitization (positive skin prick test or specific ige
    Descrição

    allergic sensitization

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C3662483
    UMLS CUI [2]
    C0430561
    subject's guardian/parent should be able to complete a symptom score on behalf of the subject.
    Descrição

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

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C1321605
    subject's guardian/parent should be able to send a symptom score weekly by sms
    Descrição

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

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C1321605
    both parents have to give written informed consent to participate in the study
    Descrição

    written informed consent

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Descrição

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    received any investigational study medication in the 4 weeks prior to screening visit
    Descrição

    investigational drug

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0013230
    UMLS CUI [1,2]
    C0040223
    significant comorbidity such as concurrent infection, history of prematurity, history of bronchopulmonary dysplasia, cystic fibrosis, other chronic lung diseases, and other severe chronic diseases
    Descrição

    significant comorbidity

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0009488
    acute asthma exacerbation within 4 weeks of screening visit
    Descrição

    asthma exacerbation

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0349790
    UMLS CUI [1,2]
    C0040223
    hospitalization within 12 weeks of screening visit
    Descrição

    hospitalization

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0019993
    UMLS CUI [1,2]
    C0040223
    systemic corticosteroids within 12 weeks of screening visit
    Descrição

    systemic corticosteroids

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C4039704
    oral corticosteroid dependence
    Descrição

    oral corticosteroid dependence

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0001617
    UMLS CUI [1,2]
    C0442027
    UMLS CUI [1,3]
    C0439857

    Similar models

    Eligibility Asthma NCT00562991

    1. StudyEvent: Eligibility
      1. Eligibility Asthma NCT00562991
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    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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