ID

34559

Beschrijving

An Observational Study of RoActemra (Tocilizumab) in Patients With Active Rheumatoid Arthritis and an Inadequate Response to Non-Biological DMARDs; ODM derived from: https://clinicaltrials.gov/show/NCT01617005

Link

https://clinicaltrials.gov/show/NCT01617005

Trefwoorden

  1. 19-01-19 19-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

19 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Rheumatoid Arthritis NCT01617005

Eligibility Rheumatoid Arthritis NCT01617005

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 (eular criteria)
Beschrijving

ID.2

Datatype

boolean

inadequate response to dmards
Beschrijving

ID.3

Datatype

boolean

initiating treatment with roactemra according to summary of product characteristics (spc)
Beschrijving

ID.4

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating females
Beschrijving

ID.5

Datatype

boolean

rheumatic autoimmune disease other than rheumatoid arthritis
Beschrijving

ID.6

Datatype

boolean

prior history or current inflammatory joint disease other than rheumatoid arthritis
Beschrijving

ID.7

Datatype

boolean

previous treatment with any biological drug used in the treatment of rheumatoid arthritis
Beschrijving

ID.8

Datatype

boolean

previous treatment with roactemra/actemra
Beschrijving

ID.9

Datatype

boolean

any contraindication to treatment with roactemra/actemra
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Rheumatoid Arthritis NCT01617005

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 (eular criteria)
boolean
ID.3
Item
inadequate response to dmards
boolean
ID.4
Item
initiating treatment with roactemra according to summary of product characteristics (spc)
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
pregnant or lactating females
boolean
ID.6
Item
rheumatic autoimmune disease other than rheumatoid arthritis
boolean
ID.7
Item
prior history or current inflammatory joint disease other than rheumatoid arthritis
boolean
ID.8
Item
previous treatment with any biological drug used in the treatment of rheumatoid arthritis
boolean
ID.9
Item
previous treatment with roactemra/actemra
boolean
ID.10
Item
any contraindication to treatment with roactemra/actemra
boolean

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