An Open Single Arm Clinical Trial to determine the therapeutic effectiveness of uloga suttigai (Metal Cauterization) in the management of kuthikaal vaatham (Achilles Tendon Bursitis)
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- To assess the improvement in the clinical symptoms like pain, swelling, tenderness, soft inflamed nodule, difficulty in walking using Subjective parameter (VAS Scale), Objective parameter (Swelling, Tenderness) and foot -ankle disability scale
研究概览
简要总结
This study is conducted To assess the improvement in the clinical symptoms like pain, swelling, tenderness, soft inflamed nodule, difficulty in walking using Subjective parameter (VAS Scale), Objective parameter (Swelling, Tenderness) and foot -ankle disability scale
Study design: An open single arm clinical trial
Patients reporting with symptoms will be subjected to screening test and documented. The patients who were enrolled will be informed about the procedure. All the enrolled patients were given researchers phone number for easily contact the researcher for clearing their doubts and any complaints arises during the trial. Complete clinical history, complaints and duration, examination findings and laboratory investigations—will be recorded in the prescribed proforma. The patient will be followed up for the treatment duration.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients with the signs and symptoms of Pain Swelling Soft inflamed nodule Patients who are willing to give routine blood investigations Patients who are willing to participate in the study by signing the consent by fulfilling the conditions of proforma.
排除标准
- •K/C/O Uncontrolled diabetes and hypertension K/C/O Rheumatoid arthritis Fracture of ankle joint K/C/O Septic arthritis Completely ruptured tendon and ligaments of ankle joints K/C/O gouty arthritis K/C/O Psoriatic arthritis K/C/O Keloid Patients who are not willing to undergo suttigai therapy Patients who are not willing to give blood samples for routine investigations Pregnant & lactating women and psychiatric patients.
结局指标
主要结局
To assess the improvement in the clinical symptoms like pain, swelling, tenderness, soft inflamed nodule, difficulty in walking using Subjective parameter (VAS Scale), Objective parameter (Swelling, Tenderness) and foot -ankle disability scale
时间窗: 48 days
次要结局
未报告次要终点
研究者
MLavanya
National institute of siddha