Efficacy of Lodotra®(Prednisone) in Reduction of Morning Stiffness Duration(K-IMPROvE)
Status:
Completed
Trial end date:
2015-04-01
Target enrollment:
Participant gender:
Summary
This study is multicenter, Ph IV, single arm, interventional study to assess relative
reduction of morning stiffness of Lodotra® in Rheumatoid Arthritis patients.Study medication
will start after study visit at baseline (week 0, visit 1) and follow-up visit will be after
2, 6 and 12 weeks after treatment (visit 2,3,4).