ID

34560

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT01667458

Trefwoorden

  1. 19-01-19 19-01-19 -
  2. 09-02-20 09-02-20 - Christian Arras
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

19 januari 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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Eligibility Rheumatoid Arthritis NCT01667458

Eligibility Rheumatoid Arthritis NCT01667458

Inclusion Criteria
Beschrijving

Inclusion Criteria

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

ID.1

Datatype

boolean

moderate to severe active rheumatoid arthritis, defined as das28 >/= 3.7
Beschrijving

ID.2

Datatype

boolean

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
Beschrijving

ID.3

Datatype

boolean

eligible for roactemra/actemra treatment in daily clinical practice
Beschrijving

ID.4

Datatype

boolean

absence of evolutive tuberculosis (tb)
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

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

ID.6

Datatype

boolean

active, severe infections
Beschrijving

ID.7

Datatype

boolean

pregnant or lactating women
Beschrijving

ID.8

Datatype

boolean

participation in any other interventional study
Beschrijving

ID.9

Datatype

boolean

patients with major depression
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Rheumatoid Arthritis NCT01667458

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
adult patients, >/= 18 years of age
boolean
ID.2
Item
moderate to severe active rheumatoid arthritis, defined as das28 >/= 3.7
boolean
ID.3
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
ID.4
Item
eligible for roactemra/actemra treatment in daily clinical practice
boolean
ID.5
Item
absence of evolutive tuberculosis (tb)
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
hypersensitivity to tocilizumab or any of the excipients
boolean
ID.7
Item
active, severe infections
boolean
ID.8
Item
pregnant or lactating women
boolean
ID.9
Item
participation in any other interventional study
boolean
ID.10
Item
patients with major depression
boolean

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