ID

34300

Descrizione

A Study of the Efficacy and Safety of Adalimumab in Pediatric Subjects With Enthesitis Related Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT01166282

collegamento

https://clinicaltrials.gov/show/NCT01166282

Keywords

  1. 16/01/19 16/01/19 -
Titolare del copyright

see on clinicaltrials.gov

Caricato su

16 gennaio 2019

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

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Eligibility Enthesitis Related Arthritis (ERA) NCT01166282

Eligibility Enthesitis Related Arthritis (ERA) NCT01166282

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of enthesitis related arthritis (era) as defined by international league of associations for rheumatology (ilar);
Descrizione

ID.1

Tipo di dati

boolean

disease activity defined as at least 3 active joints and evidence of enthesitis in at least one location;
Descrizione

ID.2

Tipo di dati

boolean

inadequate response or intolerance to at least one nonsteroidal anti-inflammatory drug and at least one disease modifying anti-rheumatic drug, either sulfasalazine or methotrexate.
Descrizione

ID.3

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
any ilar juvenile idiopathic arthritis (jia) subtype other than era;
Descrizione

ID.4

Tipo di dati

boolean

psoriasis or a history of psoriasis in the patient or first-degree relative;
Descrizione

ID.5

Tipo di dati

boolean

presence of immunoglobulin m (igm) rheumatoid factor;
Descrizione

ID.6

Tipo di dati

boolean

presence of systemic jia,
Descrizione

ID.7

Tipo di dati

boolean

history of inflammatory bowel disease, previous biologic therapy including anti-tnf therapy with a potential impact on pediatric era;
Descrizione

ID.8

Tipo di dati

boolean

infection(s) requiring treatment with iv anti-infectives within 30 days prior to baseline or oral anti-infectives within 14 days prior to baseline
Descrizione

ID.9

Tipo di dati

boolean

Similar models

Eligibility Enthesitis Related Arthritis (ERA) NCT01166282

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
diagnosis of enthesitis related arthritis (era) as defined by international league of associations for rheumatology (ilar);
boolean
ID.2
Item
disease activity defined as at least 3 active joints and evidence of enthesitis in at least one location;
boolean
ID.3
Item
inadequate response or intolerance to at least one nonsteroidal anti-inflammatory drug and at least one disease modifying anti-rheumatic drug, either sulfasalazine or methotrexate.
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
any ilar juvenile idiopathic arthritis (jia) subtype other than era;
boolean
ID.5
Item
psoriasis or a history of psoriasis in the patient or first-degree relative;
boolean
ID.6
Item
presence of immunoglobulin m (igm) rheumatoid factor;
boolean
ID.7
Item
presence of systemic jia,
boolean
ID.8
Item
history of inflammatory bowel disease, previous biologic therapy including anti-tnf therapy with a potential impact on pediatric era;
boolean
ID.9
Item
infection(s) requiring treatment with iv anti-infectives within 30 days prior to baseline or oral anti-infectives within 14 days prior to baseline
boolean

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