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临床试验/NCT05470244
NCT05470244已完成不适用

Effects of Transcutaneous Electrical Nerve Stimulation in Post-operative Total Knee Arthroplasty Recovery and Intra-venous Analgesics Requirement

University of Lahore2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年7月13日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60
试验地点
2
主要终点
Pain Intensity

研究概览

简要总结

Total knee arthroplasty (TKA) is among the major advancements for the treatment of knee pain and improvement of physical function when conservative management fails to comply with. The success of this arthoplasty results in more functional mobility and better quality of life. However, management of pain after TKA in post-operative period is a big challenge to deal.

详细描述

Transcutaneous electrical nerve stimulation is a cost effective, non-invasive electrotherapeutic modality used in alleviating pain in both acute and chronic conditions affecting neuromusculoskeletal system of the body.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

The outcome assessor will be unaware of the treatment group

入排标准

年龄范围
31 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Both male and female
  • Aged between 31-70 years
  • Total Knee Arthoplasty, who had been diagnosed with knee osteoarthritis, inflammatory arthritis, trauma, fracture result in total knee arthoplasty.

排除标准

  • Any allergic condition of skin
  • Chronic consumption of opioids
  • History of dysplasia or malignancy to knee joint
  • Any major bone operation of lower limb
  • BMI higher than 35 kg m-2
  • History of mental disorder
  • Neurological illness e.g. Alzheimer which might interfere with assessment process.

结局指标

主要结局

Pain Intensity

时间窗: Pain intensity will be measured at baseline,and change in pain intensity will be measured from baseline to 24 hour, 48 hour and 72 hours.

Pain intensity will be measured using Visual Analogue Scale

Rang of Motion

时间窗: Knee Range of Motion will be measured at baseline, and Change in Knee Range of Motion will be measured from baseline to 24 hour, 48 hour and 72 hours

Knee Rang of Motion will be measured using Universal Goniometer

Intra-venous analgesic requirement

时间窗: Analgesics requirement will be observed at first post-operative day, at second post-operative day, at third post-operative day

Dose and frequency of intravenous analgesic requirement will be observed through Patient's file

次要结局

  • Length of Hospital Stay(It will be measured from the time of randomization till the time of discharge from hospital upto ten days)

研究者

发起方
University of Lahore
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ayesha Jamil

Assistant Professor

University of Lahore

研究点 (2)

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