ID

34555

Beschrijving

A Study of RoActemra/Actemra (Tocilizumab) in Combination With DMARDs Versus Current Best Practice DMARD Therapy in Patients With Rheumatoid Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT01251120

Link

https://clinicaltrials.gov/show/NCT01251120

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 NCT01251120

Eligibility Rheumatoid Arthritis NCT01251120

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult patients, over the age of 18 years
Beschrijving

ID.1

Datatype

boolean

diagnosis of moderate-to-severe active early rheumatoid arthritis (ra) of less than 2 years duration
Beschrijving

ID.2

Datatype

boolean

das28 >3.2
Beschrijving

ID.3

Datatype

boolean

swollen joint count (sjc) >/=6 (66 joint count), and tender joint count (tjc) >/=6 (68 joint count)
Beschrijving

ID.4

Datatype

boolean

patients who have received dmards (including methotrexate) for 3-7 months
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
major surgery (including joint surgery) within 8 weeks prior to screening or planned major surgery within 6 months after baseline
Beschrijving

ID.6

Datatype

boolean

rheumatic autoimmune disease other than rheumatoid arthritis (secondary sjögrens syndrome or nodulosis with ra is permitted)
Beschrijving

ID.7

Datatype

boolean

functional class iii or iv as defined by acr classification of functional status in rheumatoid arthritis
Beschrijving

ID.8

Datatype

boolean

prior history of or current inflammatory joint disease other than ra
Beschrijving

ID.9

Datatype

boolean

Similar models

Eligibility Rheumatoid Arthritis NCT01251120

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
adult patients, over the age of 18 years
boolean
ID.2
Item
diagnosis of moderate-to-severe active early rheumatoid arthritis (ra) of less than 2 years duration
boolean
ID.3
Item
das28 >3.2
boolean
ID.4
Item
swollen joint count (sjc) >/=6 (66 joint count), and tender joint count (tjc) >/=6 (68 joint count)
boolean
ID.5
Item
patients who have received dmards (including methotrexate) for 3-7 months
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
major surgery (including joint surgery) within 8 weeks prior to screening or planned major surgery within 6 months after baseline
boolean
ID.7
Item
rheumatic autoimmune disease other than rheumatoid arthritis (secondary sjögrens syndrome or nodulosis with ra is permitted)
boolean
ID.8
Item
functional class iii or iv as defined by acr classification of functional status in rheumatoid arthritis
boolean
ID.9
Item
prior history of or current inflammatory joint disease other than ra
boolean

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