0 Évaluations
ID

39677

Description

An Observational Study on Fatigue in Patients With Rheumatoid Arthritis Treated With RoActemra/Actemra (Tocilizumab); ODM derived from: https://clinicaltrials.gov/show/NCT01667458

Lien

https://clinicaltrials.gov/show/NCT01667458

Mots-clés

Versions (2)
  1. 19/01/2019 19/01/2019 -
  2. 09/02/2020 09/02/2020 - Christian Arras
Détendeur de droits

Hoffmann-La Roche

Téléchargé le

9 février 2020

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
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    Eligibility Rheumatoid Arthritis NCT01667458

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    Eligibility Rheumatoid Arthritis NCT01667458

    1 Formulaires  
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    adult patients, >/= 18 years of age
    Description

    Age

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    moderate to severe active rheumatoid arthritis, defined as DAS28 >/= 3.7
    Description

    moderate to severe active rheumatoid arthritis, disease activity, DAS28

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C2368567
    UMLS CUI [2,1]
    C0003873
    UMLS CUI [2,2]
    C0205082
    UMLS CUI [3]
    C4481729
    inadequate clinical response to current treatment with >/= 2 non-biologic dmards, 1 of them being methotrexate optimally administered for >/= 3 months, or inadequate clinical response to anti-tnf therapy
    Description

    Clinical response to DMARD + Methotrexate or Anti-TNF therapy, inadequate

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0242708
    UMLS CUI [1,2]
    C0332257
    UMLS CUI [1,3]
    C0025677
    UMLS CUI [1,4]
    C1704632
    UMLS CUI [1,5]
    C0205412
    UMLS CUI [2,1]
    C0281481
    UMLS CUI [2,2]
    C1704632
    UMLS CUI [2,3]
    C0205412
    eligible for roactemra/actemra treatment in daily clinical practice
    Description

    Eligible Roactemra, Eligible Actemra

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C1548635
    UMLS CUI [1,2]
    C3272237
    UMLS CUI [2,1]
    C1548635
    UMLS CUI [2,2]
    C2740854
    absence of evolutive tuberculosis (tb)
    Description

    Tuberculosis, Absent

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0041296
    UMLS CUI [1,2]
    C0332197
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    hypersensitivity to tocilizumab or any of the excipients
    Description

    Hypersensitivity, Tocilicumab or other excipients

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0020517
    UMLS CUI [1,2]
    C1609165
    UMLS CUI [2,1]
    C0020517
    UMLS CUI [2,2]
    C0015237
    active, severe infections
    Description

    Active Infections

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0009450
    UMLS CUI [1,2]
    C0205082
    pregnant or lactating women
    Description

    Pregnant, lactating

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2]
    C0006147
    participation in any other interventional study
    Description

    Study Participation, Interventional Study

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C2348568
    UMLS CUI [1,2]
    C3274035
    patients with major depression
    Description

    Depression

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1269683
    Retour au début de la page

    Similar models

    Eligibility Rheumatoid Arthritis NCT01667458

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Age
    Item
    adult patients, >/= 18 years of age
    boolean
    C0001779 (UMLS CUI [1])
    moderate to severe active rheumatoid arthritis, disease activity, DAS28
    Item
    moderate to severe active rheumatoid arthritis, defined as DAS28 >/= 3.7
    boolean
    C2368567 (UMLS CUI [1])
    C0003873 (UMLS CUI [2,1])
    C0205082 (UMLS CUI [2,2])
    C4481729 (UMLS CUI [3])
    Clinical response to DMARD + Methotrexate or Anti-TNF therapy, inadequate
    Item
    inadequate clinical response to current treatment with >/= 2 non-biologic dmards, 1 of them being methotrexate optimally administered for >/= 3 months, or inadequate clinical response to anti-tnf therapy
    boolean
    C0242708 (UMLS CUI [1,1])
    C0332257 (UMLS CUI [1,2])
    C0025677 (UMLS CUI [1,3])
    C1704632 (UMLS CUI [1,4])
    C0205412 (UMLS CUI [1,5])
    C0281481 (UMLS CUI [2,1])
    C1704632 (UMLS CUI [2,2])
    C0205412 (UMLS CUI [2,3])
    Eligible Roactemra, Eligible Actemra
    Item
    eligible for roactemra/actemra treatment in daily clinical practice
    boolean
    C1548635 (UMLS CUI [1,1])
    C3272237 (UMLS CUI [1,2])
    C1548635 (UMLS CUI [2,1])
    C2740854 (UMLS CUI [2,2])
    Tuberculosis, Absent
    Item
    absence of evolutive tuberculosis (tb)
    boolean
    C0041296 (UMLS CUI [1,1])
    C0332197 (UMLS CUI [1,2])
    Item Group
    C0680251 (UMLS CUI)
    Hypersensitivity, Tocilicumab or other excipients
    Item
    hypersensitivity to tocilizumab or any of the excipients
    boolean
    C0020517 (UMLS CUI [1,1])
    C1609165 (UMLS CUI [1,2])
    C0020517 (UMLS CUI [2,1])
    C0015237 (UMLS CUI [2,2])
    Active Infections
    Item
    active, severe infections
    boolean
    C0009450 (UMLS CUI [1,1])
    C0205082 (UMLS CUI [1,2])
    Pregnant, lactating
    Item
    pregnant or lactating women
    boolean
    C0032961 (UMLS CUI [1])
    C0006147 (UMLS CUI [2])
    Study Participation, Interventional Study
    Item
    participation in any other interventional study
    boolean
    C2348568 (UMLS CUI [1,1])
    C3274035 (UMLS CUI [1,2])
    Depression
    Item
    patients with major depression
    boolean
    C1269683 (UMLS CUI [1])
    Retour au début de la page 

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