The aim of this study is to offer patients two treatment options: morning or evening administration of a JAK inhibitor prescribed within the framework of its marketing authorization, according to the EULAR response. The objective is to determine whether evening administration in our patients with rheumatoid arthritis provides greater efficacy than morning administration in our patients taking JAK inhibitors once daily.
Study Type
OBSERVATIONAL
Enrollment
90
Centre Hospitalier Princesse Grace
Monaco, Monaco
RECRUITINGEULAR response criteria between the two groups
Comparison of the evolution of the response rate (according to EULAR response criteria) between the two treatment modalities between the two groups (morning + evening vs evening + morning)
Time frame: From first intake to six months
Percentage of remission (DAS<2.6) or low disease activity
Time frame: 3 months and 6 months
Adverse events related to study treatment
number of adverse events between the two groups that led to a dose reduction or discontinuation of treatment
Time frame: From Baseline through study completion
Continuation of treatments
Time frame: From baseline to 3 months and from 3 months to 6 months
EULAR response at Month 3
Percentage of patients meeting EULAR response criteria after 3 months of treatment.
Time frame: from baseline to third month
EULAR response at Month 6
Percentage of patients meeting EULAR response criteria after 6 months of treatment.
Time frame: from baseline to six month
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