ID

14271

Beschrijving

Thyroid Hormones Treatment in Asthma Exacerbation; ODM derived from: https://clinicaltrials.gov/show/NCT02086799

Link

https://clinicaltrials.gov/show/NCT02086799

Trefwoorden

  1. 06-04-16 06-04-16 -
Geüploaded op

6 april 2016

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :


    Geen commentaren

    U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

    Eligibility Asthma NCT02086799

    Eligibility Asthma NCT02086799

    1. StudyEvent: Eligibility
      1. Eligibility Asthma NCT02086799
    Inclusion Criteria
    Beschrijving

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    18 years of age or older
    Beschrijving

    Age

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    known asthma
    Beschrijving

    Asthma

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0004096
    the exacerbation is defined as moderate or severe.
    Beschrijving

    Exacerbation of asthma Moderate | Exacerbation of asthma Severe

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0349790
    UMLS CUI [1,2]
    C0205081
    UMLS CUI [2,1]
    C0349790
    UMLS CUI [2,2]
    C0205082
    not currently enrolled as an active participant in another clinical trial of a medical therapy or device.
    Beschrijving

    Study Subject Participation Status

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    the patient or first degree family relative (in cases where the patient is intubated) has authorized his/her consent to participate in this trial. the patient will be asked to give his consent only after initial bronchodilator therapy
    Beschrijving

    Informed Consent Patients | Informed Consent First Degree Relative | Inhaled bronchodilator therapy

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0021430
    UMLS CUI [1,2]
    C0030705
    UMLS CUI [2,1]
    C0021430
    UMLS CUI [2,2]
    C1517194
    UMLS CUI [3]
    C0578554
    Exclusion Criteria
    Beschrijving

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    60 years of age or older
    Beschrijving

    Age

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    known thyroid disorders
    Beschrijving

    Thyroid disorders

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0162044
    subject where thyrotoxicosis is suspected
    Beschrijving

    Patient suspected of Thyrotoxicosis

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0522483
    UMLS CUI [1,2]
    C0040156
    known heart disease
    Beschrijving

    Heart Diseases

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0018799
    heart rate > 140
    Beschrijving

    heart rate

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0018810

    Similar models

    Eligibility Asthma NCT02086799

    1. StudyEvent: Eligibility
      1. Eligibility Asthma NCT02086799
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Age
    Item
    18 years of age or older
    boolean
    C0001779 (UMLS CUI [1])
    Asthma
    Item
    known asthma
    boolean
    C0004096 (UMLS CUI [1])
    Exacerbation of asthma Moderate | Exacerbation of asthma Severe
    Item
    the exacerbation is defined as moderate or severe.
    boolean
    C0349790 (UMLS CUI [1,1])
    C0205081 (UMLS CUI [1,2])
    C0349790 (UMLS CUI [2,1])
    C0205082 (UMLS CUI [2,2])
    Study Subject Participation Status
    Item
    not currently enrolled as an active participant in another clinical trial of a medical therapy or device.
    boolean
    C2348568 (UMLS CUI [1])
    Informed Consent Patients | Informed Consent First Degree Relative | Inhaled bronchodilator therapy
    Item
    the patient or first degree family relative (in cases where the patient is intubated) has authorized his/her consent to participate in this trial. the patient will be asked to give his consent only after initial bronchodilator therapy
    boolean
    C0021430 (UMLS CUI [1,1])
    C0030705 (UMLS CUI [1,2])
    C0021430 (UMLS CUI [2,1])
    C1517194 (UMLS CUI [2,2])
    C0578554 (UMLS CUI [3])
    Item Group
    C0680251 (UMLS CUI)
    Age
    Item
    60 years of age or older
    boolean
    C0001779 (UMLS CUI [1])
    Thyroid disorders
    Item
    known thyroid disorders
    boolean
    C0162044 (UMLS CUI [1])
    Patient suspected of Thyrotoxicosis
    Item
    subject where thyrotoxicosis is suspected
    boolean
    C0522483 (UMLS CUI [1,1])
    C0040156 (UMLS CUI [1,2])
    Heart Diseases
    Item
    known heart disease
    boolean
    C0018799 (UMLS CUI [1])
    heart rate
    Item
    heart rate > 140
    boolean
    C0018810 (UMLS CUI [1])

    Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

    Velden gemarkeerd met een * zijn verplicht.

    Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

    Watch Tutorial