Clinical Research Directory

Comparison of Bracing and Eccentric Loading Exercises on Pain Modulation and Functional Improvement in Acute Pes Anserine Bursitis Patients

This study aims to compare the effects of knee bracing and eccentric loading exercises on pain and functional ability in adults with acute pes anserine bursitis. Pes anserine bursitis is a condition affecting the inner side of the knee that can cause pain and difficulty with activities such as walking, climbing stairs, and standing up from a chair. A total of 32 participants will be included in the study and divided into two groups. One group will receive a knee-bracing intervention, while the other group will participate in a structured exercise program involving eccentric loading and strengthening exercises for the muscles around the knee. The bracing group will be instructed to wear a properly fitted medial-support knee brace for approximately 6-8 hours daily during weight-bearing activities. The exercise group will perform prescribed exercises three times per week for eight weeks, with exercise intensity adjusted according to individual tolerance. Pain intensity and knee-related functional ability will be assessed using the Visual Analogue Scale (VAS) and the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). Assessments will be conducted before treatment and at the planned follow-up visits to evaluate changes in symptoms and function. The findings are intended to help determine which intervention provides greater improvement in pain and functional ability in people with acute pes anserine bursitis and may help guide physiotherapy treatment decisions.

Efficacy of Platelet-rich Plasma Injection Compare With Corticosteroid in Pes Anserinus Pain Syndrome

The goal of this research is to study the efficacy of treatment between PRP injection and corticosteroid injection in patients with pes anserinus bursitis. The research question is whether PRP can reduce pain more effectively than corticosteroids. The study is divided into two groups: one group receiving PRP injections and the second group receiving corticosteroid injections. Treatment outcomes will be monitored at four time points: baseline, 4 weeks, 12 weeks, and 24 weeks. The outcomes will be measured using the VAS and WOMAC scores.