The Effect of Cilostazol on Rheumatoid Arthritis Patients
Rheumatoid Arthritis
About this trial
This is an interventional treatment trial for Rheumatoid Arthritis focused on measuring Rheumatoid Arthritis, Cilostazol
Eligibility Criteria
Inclusion Criteria: Adult patients. (>18 years old). Moderate to high disease activity (DAS28-CRP>3.2). Patients receiving stable cDMARD regimen for at least 3 months before inclusion in the study. Exclusion Criteria: Hypersensitivity to cilostazol. Heart failure. Pregnant and lactating women. Patients with liver impairment (ALT or AST > 3* ULN). Patients with renal impairment (CrCl<60 mL/min). Patients receiving any other antiplatelet or anticoagulant
Sites / Locations
- Al-Zahraa HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Cilostazol arm
Control
35 patients receiving conventional synthetic disease modifying antirheumatic drugs in addition to Cilostazol 100 mg twice daily for 6 months.
35 patients receiving conventional synthetic disease modifying antirheumatic drugs for 6 months.