ID

34562

Descripción

Biomarkers of Remission in Rheumatoid Arthritis (BioRRA); ODM derived from: https://clinicaltrials.gov/show/NCT02219347

Link

https://clinicaltrials.gov/show/NCT02219347

Palabras clave

  1. 19/1/19 19/1/19 -
  2. 15/4/20 15/4/20 -
  3. 16/4/20 16/4/20 - Sarah Riepenhausen
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

19 de enero de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0

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Eligibility Rheumatoid Arthritis NCT02219347

Eligibility Rheumatoid Arthritis NCT02219347

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
clinical diagnosis of rheumatoid arthritis made by consultant rheumatologist at least 12 months previously
Descripción

ID.1

Tipo de datos

boolean

current single or combination use of methotrexate, sulphasalazine and/or hydroxychloroquine
Descripción

ID.2

Tipo de datos

boolean

arthritis currently in remission, as judged clinically by referring healthcare professional
Descripción

ID.3

Tipo de datos

boolean

willing to consider dmard withdrawal
Descripción

ID.4

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
use of biologic therapy within the past 6 months
Descripción

ID.5

Tipo de datos

boolean

received steroids within past 3 months (enteral, parenteral or intra-articular)
Descripción

ID.6

Tipo de datos

boolean

use of any dmard other than methotrexate, sulphasalazine or hydroxychloroquine within the past 6 months (or past 12 months for leflunomide)
Descripción

ID.7

Tipo de datos

boolean

current pregnancy, or pregnancy planned within next 6 months
Descripción

ID.8

Tipo de datos

boolean

current participation within another clinical trial
Descripción

ID.9

Tipo de datos

boolean

inability to provide informed consent
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Rheumatoid Arthritis NCT02219347

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
clinical diagnosis of rheumatoid arthritis made by consultant rheumatologist at least 12 months previously
boolean
ID.2
Item
current single or combination use of methotrexate, sulphasalazine and/or hydroxychloroquine
boolean
ID.3
Item
arthritis currently in remission, as judged clinically by referring healthcare professional
boolean
ID.4
Item
willing to consider dmard withdrawal
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
use of biologic therapy within the past 6 months
boolean
ID.6
Item
received steroids within past 3 months (enteral, parenteral or intra-articular)
boolean
ID.7
Item
use of any dmard other than methotrexate, sulphasalazine or hydroxychloroquine within the past 6 months (or past 12 months for leflunomide)
boolean
ID.8
Item
current pregnancy, or pregnancy planned within next 6 months
boolean
ID.9
Item
current participation within another clinical trial
boolean
ID.10
Item
inability to provide informed consent
boolean

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