ID

40381

Description

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

Lien

https://clinicaltrials.gov/show/NCT02219347

Mots-clés

Versions (3)
  1. 19/01/2019 19/01/2019 -
  2. 15/04/2020 15/04/2020 -
  3. 16/04/2020 16/04/2020 - Sarah Riepenhausen
Détendeur de droits

Newcastle-upon-Tyne Hospitals NHS Trust

Téléchargé le

16 avril 2020

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 4.0
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Eligibility Rheumatoid Arthritis NCT02219347

Anglais

Eligibility Rheumatoid Arthritis NCT02219347

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

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

Rheumatoid arthritis disease length, judged by rheumatologist

Type de données

boolean

Alias
UMLS CUI [1,1]
C0003873
UMLS CUI [1,2]
C0872146
UMLS CUI [1,3]
C0022423
UMLS CUI [1,4]
C0334889
current single or combination use of methotrexate, sulphasalazine and/or hydroxychloroquine
Description

Methotrexate | sulfasalazine | hydroxycholoroquine | combination

Type de données

boolean

Alias
UMLS CUI [1]
C0025677
UMLS CUI [2]
C0036078
UMLS CUI [3]
C0020336
UMLS CUI [4,1]
C0025677
UMLS CUI [4,2]
C0205195
UMLS CUI [5,1]
C0036078
UMLS CUI [5,2]
C0205195
UMLS CUI [6,1]
C0020336
UMLS CUI [6,2]
C0205195
arthritis currently in remission, as judged clinically by referring healthcare professional
Description

Rheumatoid arthritis in remission, judged by health professional

Type de données

boolean

Alias
UMLS CUI [1,1]
C0003873
UMLS CUI [1,2]
C0544452
UMLS CUI [1,3]
C0022423
UMLS CUI [1,4]
C1704312
willing to consider dmard withdrawal
Description

Willing to consider DMARD withdrawal

Type de données

boolean

Alias
UMLS CUI [1,1]
C0242708
UMLS CUI [1,2]
C2349954
UMLS CUI [1,3]
C0600109
Exclusion Criteria
Description

Exclusion Criteria

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

Recent biologic therapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0005527
UMLS CUI [1,2]
C0332185
received steroids within past 3 months (enteral, parenteral or intra-articular)
Description

Recent enteral, parenteral or intra-articular steroid therapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0574135
UMLS CUI [1,2]
C0332185
UMLS CUI [2,1]
C3840673
UMLS CUI [2,2]
C0332185
UMLS CUI [3,1]
C2064783
UMLS CUI [3,2]
C0332185
use of any dmard other than methotrexate, sulphasalazine or hydroxychloroquine within the past 6 months (or past 12 months for leflunomide)
Description

Recent use of DMARDs except for methotrexate, sulphasalazine or hydroxychloroquine

Type de données

boolean

Alias
UMLS CUI [1,1]
C0242708
UMLS CUI [1,2]
C0332185
UMLS CUI [2,1]
C0025677
UMLS CUI [2,2]
C0332300
UMLS CUI [3,1]
C0036078
UMLS CUI [3,2]
C0332300
UMLS CUI [4,1]
C0020336
UMLS CUI [4,2]
C0332300
current pregnancy, or pregnancy planned within next 6 months
Description

Pregnancy, current or planned

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
current participation within another clinical trial
Description

Study Subject Participation Status

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
inability to provide informed consent
Description

Informed consent Unable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
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Similar models

Eligibility Rheumatoid Arthritis NCT02219347

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Rheumatoid arthritis disease length, judged by rheumatologist
Item
clinical diagnosis of rheumatoid arthritis made by consultant rheumatologist at least 12 months previously
boolean
C0003873 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C0022423 (UMLS CUI [1,3])
C0334889 (UMLS CUI [1,4])
Methotrexate | sulfasalazine | hydroxycholoroquine | combination
Item
current single or combination use of methotrexate, sulphasalazine and/or hydroxychloroquine
boolean
C0025677 (UMLS CUI [1])
C0036078 (UMLS CUI [2])
C0020336 (UMLS CUI [3])
C0025677 (UMLS CUI [4,1])
C0205195 (UMLS CUI [4,2])
C0036078 (UMLS CUI [5,1])
C0205195 (UMLS CUI [5,2])
C0020336 (UMLS CUI [6,1])
C0205195 (UMLS CUI [6,2])
Rheumatoid arthritis in remission, judged by health professional
Item
arthritis currently in remission, as judged clinically by referring healthcare professional
boolean
C0003873 (UMLS CUI [1,1])
C0544452 (UMLS CUI [1,2])
C0022423 (UMLS CUI [1,3])
C1704312 (UMLS CUI [1,4])
Willing to consider DMARD withdrawal
Item
willing to consider dmard withdrawal
boolean
C0242708 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Recent biologic therapy
Item
use of biologic therapy within the past 6 months
boolean
C0005527 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
Recent enteral, parenteral or intra-articular steroid therapy
Item
received steroids within past 3 months (enteral, parenteral or intra-articular)
boolean
C0574135 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
C3840673 (UMLS CUI [2,1])
C0332185 (UMLS CUI [2,2])
C2064783 (UMLS CUI [3,1])
C0332185 (UMLS CUI [3,2])
Recent use of DMARDs except for methotrexate, sulphasalazine or hydroxychloroquine
Item
use of any dmard other than methotrexate, sulphasalazine or hydroxychloroquine within the past 6 months (or past 12 months for leflunomide)
boolean
C0242708 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
C0025677 (UMLS CUI [2,1])
C0332300 (UMLS CUI [2,2])
C0036078 (UMLS CUI [3,1])
C0332300 (UMLS CUI [3,2])
C0020336 (UMLS CUI [4,1])
C0332300 (UMLS CUI [4,2])
Pregnancy, current or planned
Item
current pregnancy, or pregnancy planned within next 6 months
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Study Subject Participation Status
Item
current participation within another clinical trial
boolean
C2348568 (UMLS CUI [1])
Informed consent Unable
Item
inability to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
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