ID

34562

Descrição

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

Link

https://clinicaltrials.gov/show/NCT02219347

Palavras-chave

  1. 19/01/2019 19/01/2019 -
  2. 15/04/2020 15/04/2020 -
  3. 16/04/2020 16/04/2020 - Sarah Riepenhausen
Titular dos direitos

see on clinicaltrials.gov

Transferido a

19 de janeiro de 2019

DOI

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Licença

Creative Commons BY-NC 3.0

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Eligibility Rheumatoid Arthritis NCT02219347

Eligibility Rheumatoid Arthritis NCT02219347

Inclusion Criteria
Descrição

Inclusion Criteria

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

ID.1

Tipo de dados

boolean

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

ID.2

Tipo de dados

boolean

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

ID.3

Tipo de dados

boolean

willing to consider dmard withdrawal
Descrição

ID.4

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

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

ID.5

Tipo de dados

boolean

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

ID.6

Tipo de dados

boolean

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

ID.7

Tipo de dados

boolean

current pregnancy, or pregnancy planned within next 6 months
Descrição

ID.8

Tipo de dados

boolean

current participation within another clinical trial
Descrição

ID.9

Tipo de dados

boolean

inability to provide informed consent
Descrição

ID.10

Tipo de dados

boolean

Similar models

Eligibility Rheumatoid Arthritis NCT02219347

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