跳至主要内容
临床试验/CTRI/2017/04/008382
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

Jamia Hamdard0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中
发起方
Jamia Hamdard
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

发起方
Jamia Hamdard

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