tofacitinib
DrugPatients received tofacitinib for the treatment of juvenile idiopathic arthritis (JIA).
NCT Number: NCT07211932
This study aims to evaluate, using real-world clinical practice data, the efficacy of tofacitinib in improving the clinical control of juvenile idiopathic arthritis (JIA) after 12 months of treatment.
Trial opening soon.
Get NotifiedUp to 18 year
All sexes
Observational
Hospital Sant Joan de Déu Barcelona, Barcelona, Spain
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Diagnosis of juvenile idiopathic arthritis (JIA) documented in the medical record by the treating rheumatologist.
Documentation in the medical record of the medical indication for tofacitinib treatment, with a diagnostic justification related to JIA.
Age under 18 years at the time of the treatment indication with tofacitinib.
Exclusion criteria
Participants diagnosed with any of the following conditions:
Reactive arthritis
Arthritis associated with inflammatory bowel disease
Arthritis associated with another autoimmune disease
Patients received tofacitinib for the treatment of juvenile idiopathic arthritis (JIA).
Time frame: Baseline and 12 months
Change in the Juvenile Arthritis Disease Activity Score (JADAS-10) score at 12 months of treatment with tofacitinib. Range score: 0 to 10, the less score the better
Contact information is provided by the study sponsor or research team.
Consorci Sanitari de l'Alt Penedès i Garraf
Other
Efficacy of Tofacitinib in Patients With Juvenile Idiopathic Arthritis: A Study Based on Real-world Clinical Practice Data.
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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