ID

34559

Description

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

Keywords

  1. 1/19/19 1/19/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 19, 2019

DOI

To request one please log in.

License

Creative Commons BY 4.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Rheumatoid Arthritis NCT01617005

Eligibility Rheumatoid Arthritis NCT01617005

Inclusion Criteria
Description

Inclusion Criteria

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

ID.1

Data type

boolean

moderate to severe active rheumatoid arthritis (eular criteria)
Description

ID.2

Data type

boolean

inadequate response to dmards
Description

ID.3

Data type

boolean

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

ID.4

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating females
Description

ID.5

Data type

boolean

rheumatic autoimmune disease other than rheumatoid arthritis
Description

ID.6

Data type

boolean

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

ID.7

Data type

boolean

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

ID.8

Data type

boolean

previous treatment with roactemra/actemra
Description

ID.9

Data type

boolean

any contraindication to treatment with roactemra/actemra
Description

ID.10

Data type

boolean

Similar models

Eligibility Rheumatoid Arthritis NCT01617005

Name
Type
Description | Question | Decode (Coded Value)
Data type
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

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial