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临床试验/NCT06240845
NCT06240845已完成不适用

Effect of High Versus Low-level Laser Therapy in Patients of Lumber Radiculopathy

Riphah International University4 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2023年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
38
试验地点
4
主要终点
Level of Disability

研究概览

简要总结

To Compare the effects of high-level laser therapy (HLLT) and low-level laser therapy (LLLT) on pain in patients with lumbar radiculopathy.

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
Double (Participant, Investigator)

入排标准

年龄范围
40 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients of both genders male and female will be included.
  • Patients aged 40-65 years will be included.
  • Patients with a diagnosis of lumbar radiculopathy confirmed by clinical evaluation by a physician or physiotherapist.
  • Patients with a history of radicular leg pain and/or numbness or tingling sensation in the leg.
  • a positive score on the Straight Leg Raise (pain between 35 degrees and 75 degrees), pain limiting functional ability, and scores at least 3/10 on the VAS, restricted lumbar range of motion - 25% flexion, 20% extension.
  • Patients who have not received any form of treatment for lumbar radiculopathy within the past 3 months

排除标准

  • Patients with a history of spinal surgery in the last 2 years or spinal deformity.
  • Patients with a history of fracture or dislocation of the lumbar spine.
  • Patients with a diagnosis of any other neurological disorder or neuropathy.
  • Patients who are pregnant or breastfeeding.
  • Patients with any other medical condition that may interfere i.e. inflammatory rheumatic disease, cardiac pacemaker, continuing that may interfere with the study outcomes or put them at risk with the study outcomes or put them at risk.

结局指标

主要结局

Level of Disability

时间窗: 6 weeks

Oswestry Disability Index (ODI)

To measure Quality of Life

时间窗: 6 weeks

Health Questionnaire (EQ-5D-5L)

Pain Level

时间窗: 6 weeks

Visual Analogue scale

Rang of motion

时间窗: 6 weeks

Straight Leg Raise

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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