An Open Clinical Study to evaluate the clinical efficacy of siddha sasthric formulation "PANJALAVANA PARPAM"(Internal)"LAHU VATHA KESARI THYLAM " for the treatment of AZHAL KEEL VAYU.
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Reduction In Severity Of Joint Pain,Stiffness,And Improvement In Physical Functioning And Quality Of Life
研究概览
简要总结
Phase IIcriteria based clinical study to evaluate the clinical efficacy of siddha herbomineral formulation of Panja lavana parpam 1 Kalanju (5.1Gram) Bd with ¼ Perungayam added toHoney (Internal) andlahuvatha kesari thylam 30 ml (External) on Azal keel vayu(Osteo arthritis) for 48 daysin 40 patients during the trial period of 1 year 6 months that will beconducted in government siddha medical college palyamkottai tamil nadu theprimary out come is reducing the clinical symptoms and increasing the range ofmovements of trail drug Panja lavana parpam (Internal) and lahu vatha kesari thylam (external) the secondary outcome will be the Evaluation of siddha diagnosticparameters.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Open Label
入排标准
- 年龄范围
- 30.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •1.patients having symptoms of joint pain in one or both knee 2.joints,swelling,tenderness,stiffness,crepitation,restricted movements of joints.
- •3.patients who are willing to take x-ray before and after treatment.
- •4.patients who are willing to participate in this study with knowledge of potential risk.
排除标准
- •1.systemic illness of the patient 2.Rhematoid arthritis 3.Use of narcotic drug 4.Pregnancy and lactation 5.History of trauma 6.Carcinoma patient Tuberculosis Immuno compromised patients Clinically significant abnormal laboratory values.
结局指标
主要结局
Reduction In Severity Of Joint Pain,Stiffness,And Improvement In Physical Functioning And Quality Of Life
时间窗: 48 days
次要结局
- Evaluation of siddha diagnostic parameters(48 days)