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临床试验/CTRI/2024/02/062318
CTRI/2024/02/062318尚未招募不适用

Effect of Radial Extracorporeal Shockwave Therapy v/s Therapeutic Ultrasound on pain, physical function and strength in patients with Knee Osteoarthritis: An Experimental Study

K J Somaiya college of physiotherapy1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2024年2月25日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
50
试验地点
1
主要终点
1)Visual analogue scale

研究概览

简要总结

Approval is obtained from Institutional Ethics Committee. Patients will be selected based on inclusion criteria. Written Informed Consent will be taken from patients and basic demographic data will be collected. Pre-treatment assessment will be done for pain using  Visual Analogue Scale (VAS),  for physical function using  WOMAC scale and  strength using  isokinetic dynamometer.

Patients will be allocated randomly using computer based software into Group A or Group B. Group A – Radial Extracorporeal Shockwave therapy+ Exercise for 3 weeks. Group B -Therapeutic ultrasound+ Exercises for 3 weeks. Post treatment Assessment will be done after 3 weeks  for pain using Visual Analogue Scale (VAS),  for physical function using WOMAC scale and  strength using  isokinetic.Statistical analysis will be done after data collection.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
40.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients between 40 to 60 years of age, diagnosed with osteoarthritis of the knee with a Kellgren-Lawrence grading of II or III, having unilateral knee osteoarthritis or more severe symptoms in one knee of bilateral osteoarthritis, experiencing pain in the knee joint with a visual analog scale (VAS) score ranging from 4 to 7, and willing to participate in the study.

排除标准

  • Previous knee surgery (in last 2 years).
  • Knee joint infection.
  • Metal implants.
  • Rheumatoid arthritis or other inflammatory joint diseases.
  • Knee joint instability or ligamentous injury.
  • Contraindication to Shock wave therapy or Therapeutic ultrasound.
  • Any other medical or psychological condition that may interfere with the study procedures or outcome.

结局指标

主要结局

1)Visual analogue scale

时间窗: Pre intervention:Baseline assessment | Post intervention:After 3 weeks

2)Western Ontario and McMaster University Osteoarthritis Scale

时间窗: Pre intervention:Baseline assessment | Post intervention:After 3 weeks

3)Humac NORM Isokinetic Dynamometer

时间窗: Pre intervention:Baseline assessment | Post intervention:After 3 weeks

次要结局

未报告次要终点

研究者

发起方
K J Somaiya college of physiotherapy
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Niraj Khandelwal

K J Somaiya college of physiotherapy

研究点 (1)

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