CTRI/2017/01/007691已完成2 期
Evaluation of the effect of Upanaha treatment with Vachadi Upanaha Churna in Osteoarthritis (OA Knee) wrt pain and stiffness of joints - Upanaha
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.Patients of either sex aged between 35 and 65 years.
- •2.Subjects having VAS score for knee pain between 45-74 mm (moderate pain)
- •3.Clinical and radiological evidence of Osteoarthritis knee (Unilateral/ bilateral) as per ACR criteria
- •(i)knee pain,
- •(ii)at least one of three
- •(a)Age > 50 years
- •(b)stiffness < 30 minutes
- •(c)Crepitus
- •(iii)Osteophytes
- •4.Radiographical changes as per Grade I to III of Kellgren& Lawrence Radiological scale
- •5.Able and willing to participate and provide signed informed consent
排除标准
- •1.Patients with Grade IV Kellgren& Lawrence Radiological scale
- •2.History of any trauma/ fractured joint / surgical/diagnostic intervention with reference to the affected joint(s).
- •3.H/O monoarthritis/ polyarthritis other than Osteoarthritis Knee such as gouty arthritis, rheumatoid arthritis and psoriatic arthritis etc.
- •4.Any unstable cardio-vascular disease.
- •5.Patients with uncontrolled Hypertension ( >160/100 mmHg)
- •6.Patients with uncontrolled Diabetes Mellitus having HbA1C >7.5%
- •7.Patients with evidence of malignancy.
- •8.Patients with any concurrent hepatic disorder (defined as liver enzymes SGOT/SGPT >2 times upper normal limit) or Renal Disorders (defined as S.Creatinine >1.4mg/dl) or Pulmonary Dysfunction
- •9.The patient has been administered any chondroprotective drugs, intra-articular injection into the affected joint or systemic medication with corticosteroids during the preceding 3 months.
- •10.Pregnant / lactating woman.
- •11.Patients who are currently participating in any other clinical trial.
- •12.Any other condition which the Principal Investigator thinks may jeopardize the study.
研究者
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