跳至主要内容
临床试验/CTRI/2024/06/068801
CTRI/2024/06/068801尚未招募不适用

An open clinical trial to evaluate the therapeutic effectiveness of Murivu Ennai (External) for the management of Muzhangal Mootu Savvu Kaayam (Anterior Cruciate Ligament Injury) along with Varmam Therapeutic Manipulation

National Institute of Siddha1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2024年7月25日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
20
试验地点
1
主要终点
The reduction in pain and improvement in range of motion of the affected knee after

研究概览

简要总结

An open clinical trial which will be carried out for 18 months in the OPD of Varmam Maruthuvam, Ayothidoss Pandithar Hospital, National Institute of Siddha with 20 patients as sample size. The patients will be non randomly selected based on inclusion and exclusion criteria for enrollment in the study and treated with Varma thadaval (Varma manipulation technique) with Murivu Ennai for the management of Muzhangal Mootu Savvu Kaayam weekly once for 70 days. Prognosis will be documented in the appropriate forms enclosed with the protocol. Primary outcome of the study is assessed clinically and by the KOOS survey score and the results will be statiscally analysed

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • ACL Injury Grade 1 and 2 in MRI Patients willing to undergo radiological investigation.
  • Patients willing to sign the informed consent form KOOS score in the range of 0 to 40%.

排除标准

  • Complete Anterior Cruciate ligament tear Severe Co-morbidities Pregnant and Lactating women.

结局指标

主要结局

The reduction in pain and improvement in range of motion of the affected knee after

时间窗: At baseline, 10th week

the treatment with trial drugs will be assessed by KOOS Score. The expected outcome will be

时间窗: At baseline, 10th week

above 60% with KOOS Score.

时间窗: At baseline, 10th week

次要结局

未报告次要终点

研究者

申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr M Fouziya Thasim

National Institute of Siddha

研究点 (1)

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