ID

34553

Beskrivning

A Study of Tocilizumab Plus Non-biological DMARD in Patients With Moderate to Severe Rheumatoid Arthritis and an Inadequate Response to Non-biological DMARDs; ODM derived from: https://clinicaltrials.gov/show/NCT01034397

Länk

https://clinicaltrials.gov/show/NCT01034397

Nyckelord

  1. 2019-01-19 2019-01-19 -
  2. 2019-05-21 2019-05-21 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

19 januari 2019

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Rheumatoid Arthritis NCT01034397

Eligibility Rheumatoid Arthritis NCT01034397

Inclusion Criteria
Beskrivning

Inclusion Criteria

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

ID.1

Datatyp

boolean

moderate to severe rheumatoid arthritis of >/=6 months duration
Beskrivning

ID.2

Datatyp

boolean

synovitis (swollen and tender joint) in the wrist of the dominant hand
Beskrivning

ID.3

Datatyp

boolean

non-biologic dmards at stable dose for >/=12 weeks prior to baseline
Beskrivning

ID.4

Datatyp

boolean

oral corticosteroids at stable dose for at least 25 out of 28 days prior to baseline
Beskrivning

ID.5

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
rheumatic autoimmune disease other than ra
Beskrivning

ID.6

Datatyp

boolean

history of or current inflammatory joint disease other than ra
Beskrivning

ID.7

Datatyp

boolean

functional class iv (acr classification)
Beskrivning

ID.8

Datatyp

boolean

intraarticular or parenteral corticosteroids within 6 weeks prior to baseline
Beskrivning

ID.9

Datatyp

boolean

previous treatment with a biologic agent for ra
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Rheumatoid Arthritis NCT01034397

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
adult patients, >/=18 years of age
boolean
ID.2
Item
moderate to severe rheumatoid arthritis of >/=6 months duration
boolean
ID.3
Item
synovitis (swollen and tender joint) in the wrist of the dominant hand
boolean
ID.4
Item
non-biologic dmards at stable dose for >/=12 weeks prior to baseline
boolean
ID.5
Item
oral corticosteroids at stable dose for at least 25 out of 28 days prior to baseline
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
rheumatic autoimmune disease other than ra
boolean
ID.7
Item
history of or current inflammatory joint disease other than ra
boolean
ID.8
Item
functional class iv (acr classification)
boolean
ID.9
Item
intraarticular or parenteral corticosteroids within 6 weeks prior to baseline
boolean
ID.10
Item
previous treatment with a biologic agent for ra
boolean

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