This document presents a dissertation proposal evaluating the clinical efficacy of Vriddadarvadi Loha in managing Amavata, which correlates to rheumatoid arthritis. The study will involve a minimum of 30 patients receiving 500mg of Vriddadarvadi Loha daily for 60 days. Parameters like pain, swelling, and stiffness will be assessed at baseline and on days 15, 30, 45 and 60 to analyze relief from signs and symptoms. The results will be categorized as excellent, good, moderate or mild relief based on percentage improvement.