ID

34559

Descripción

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

Palabras clave

  1. 19/1/19 19/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

19 de enero de 2019

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0

Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Rheumatoid Arthritis NCT01617005

Eligibility Rheumatoid Arthritis NCT01617005

Inclusion Criteria
Descripción

Inclusion Criteria

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

ID.1

Tipo de datos

boolean

moderate to severe active rheumatoid arthritis (eular criteria)
Descripción

ID.2

Tipo de datos

boolean

inadequate response to dmards
Descripción

ID.3

Tipo de datos

boolean

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

ID.4

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating females
Descripción

ID.5

Tipo de datos

boolean

rheumatic autoimmune disease other than rheumatoid arthritis
Descripción

ID.6

Tipo de datos

boolean

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

ID.7

Tipo de datos

boolean

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

ID.8

Tipo de datos

boolean

previous treatment with roactemra/actemra
Descripción

ID.9

Tipo de datos

boolean

any contraindication to treatment with roactemra/actemra
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Rheumatoid Arthritis NCT01617005

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

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