CTRI/2017/04/008382招募中2 期
Evaluation of efficacy and safety of Irsal-i-Alaq (Leeching) in the management of Waja-al- Rukba (Knee Osteoarthritis
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 入组人数
- 60
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
- •Patients of Knee OA in age groups of 35 years to 65 years.
- •Subjective pain intensity of 20 mm or more at baseline on Visual Analogue Scale (VAS).
- •Clinically stable patients.
- •Patients of both sexes.
- •Patients willing to sign the informed consent form and participate in the trial voluntarily.
排除标准
- •Diabetes mellitus Type 1 and uncontrolled Type 2.
- •Active hepatic disease, abnormal liver function. (Alanine transaminase, Aspartate transaminase or Total bilirubin level more than twice normal values), or renal dysfunction (blood creatinine over the upper limit of normal).
- •Current anticoagulant therapy or bleeding disorders or Severe Anaemia.
- •Pregnant and lactating mothers.
- •ESR > 40 mm/hr.
- •Terminally ill patients.
- •Patients below 35 years and above 65 years of age.
- •Patients who fail to give consent.
- •Subjects who had received leeching to the knee region 1 months prior to the study.
研究者
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