0 Bedömningar
ID

17241

Beskrivning

Obesity and Asthma:a Specific Phenotype; ODM derived from: https://clinicaltrials.gov/show/NCT00532363

Länk

https://clinicaltrials.gov/show/NCT00532363

Nyckelord

Versioner (1)
  1. 2016-09-01 2016-09-01 -
Uppladdad den

1 september 2016

DOI

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Licens

Creative Commons BY 4.0
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    Eligibility Obesity NCT00532363

    Engelsk

    Eligibility Obesity NCT00532363

    1 Formulär  
    1. StudyEvent: Eligibility
      1. Eligibility Obesity NCT00532363
    Inclusion Criteria
    Beskrivning

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    will be women aged 18 years and over
    Beskrivning

    Gender, Age

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0079399
    UMLS CUI [2]
    C0001779
    will be in good health apart from asthma or obesity as determined by history and physical examination (no other condition that could influence the proposed tests).
    Beskrivning

    Good health as determined by history and physical examination

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0018759
    UMLS CUI [2]
    C0031809
    all will be non smokers or ex-smokers for more than six months with a smoking history of no more than 10 pack- years (i.e., one pack per day or its equivalent for 10 years.)
    Beskrivning

    non smokers or ex-smokers for more than six months

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0543414
    subjects will have a physician's made diagnosis of severe asthma and treated with corticosteroids.
    Beskrivning

    severe asthma treated with corticosteroids

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0581126
    UMLS CUI [2]
    C0001617
    Exclusion Criteria
    Beskrivning

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    subjects who are, in the opinion of the investigator, mentally or legally incapacitated thus preventing informed consent from being obtained.
    Beskrivning

    Informed consent

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0021430
    UMLS CUI [1,2]
    C0439801
    UMLS CUI [1,3]
    C0009488
    subjects having a co-existing illness that precludes them from the trial.
    Beskrivning

    Comorbidity

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C1321605
    UMLS CUI [1,2]
    C0439801
    UMLS CUI [1,3]
    C0009488
    pregnancy or lactation
    Beskrivning

    Pregnancy or lactation

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2]
    C0006147
    contraindication to the prednisone treatment.
    Beskrivning

    Contraindication to prednisone treatment

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C1301624
    UMLS CUI [1,2]
    C0032952
    Tillbaka till toppen

    Similar models

    Eligibility Obesity NCT00532363

    1 Formulär
    1. StudyEvent: Eligibility
      1. Eligibility Obesity NCT00532363
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Gender, Age
    Item
    will be women aged 18 years and over
    boolean
    C0079399 (UMLS CUI [1])
    C0001779 (UMLS CUI [2])
    Good health as determined by history and physical examination
    Item
    will be in good health apart from asthma or obesity as determined by history and physical examination (no other condition that could influence the proposed tests).
    boolean
    C0018759 (UMLS CUI [1])
    C0031809 (UMLS CUI [2])
    non smokers or ex-smokers for more than six months
    Item
    all will be non smokers or ex-smokers for more than six months with a smoking history of no more than 10 pack- years (i.e., one pack per day or its equivalent for 10 years.)
    boolean
    C0543414 (UMLS CUI [1])
    severe asthma treated with corticosteroids
    Item
    subjects will have a physician's made diagnosis of severe asthma and treated with corticosteroids.
    boolean
    C0581126 (UMLS CUI [1])
    C0001617 (UMLS CUI [2])
    Item Group
    C0680251 (UMLS CUI)
    Informed consent
    Item
    subjects who are, in the opinion of the investigator, mentally or legally incapacitated thus preventing informed consent from being obtained.
    boolean
    C0021430 (UMLS CUI [1,1])
    C0439801 (UMLS CUI [1,2])
    C0009488 (UMLS CUI [1,3])
    Comorbidity
    Item
    subjects having a co-existing illness that precludes them from the trial.
    boolean
    C1321605 (UMLS CUI [1,1])
    C0439801 (UMLS CUI [1,2])
    C0009488 (UMLS CUI [1,3])
    Pregnancy or lactation
    Item
    pregnancy or lactation
    boolean
    C0032961 (UMLS CUI [1])
    C0006147 (UMLS CUI [2])
    Contraindication to prednisone treatment
    Item
    contraindication to the prednisone treatment.
    boolean
    C1301624 (UMLS CUI [1,1])
    C0032952 (UMLS CUI [1,2])
    Tillbaka till toppen 

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