跳至主要内容
临床试验/CTRI/2025/09/094992
CTRI/2025/09/094992尚未招募不适用

Combined effect of Dry Needling as an adjunct to Mechanical Traction and Neural Mobilizataion in subjects with Lumbar Radiculopathy: A RCT

Priyanka Niak1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2025年9月28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
34
试验地点
1
主要终点
1.Numeric pain rating scale

研究概览

简要总结

This randomized clinical trial investigates the combined effect of dry needling, spinal traction, and neural mobilization in patients with lumbar radiculopathy. Lumbar radiculopathy, commonly caused by disc herniation and nerve root compression, has a prevalence of 23.9% in India and 4–6% in the general population. The study will include 34 participants aged 30–50 years with radiating low back pain. Group A will receive dry needling with mechanical traction plus conventional therapy (core exercises and TENS). Group B will receive dry needling with neural mobilization plus conventional therapy. Dry needling targets lumbar paraspinal and gluteus medius trigger points to reduce pain and muscle tension. Mechanical traction helps decompress nerve roots, while neural mobilization improves femoral and sciatic nerve mobility. Conventional therapy includes stabilization exercises and TENS for pain relief. Outcome measures are pain intensity (NPRS), functional disability Modified Oswesrty disability questionnaire(MODQ), and lumbar mobility modified modified schober’s test (MMST).

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant Blinded

入排标准

年龄范围
30.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • 1.All genders between 30-50 years 2.Male and Female patients with lumbar radiculopathy and radiating to one leg.
  • 3.Clinically diagnosed case of PIVD 4.Positive SLR and femoral test 5.Willing to participate.

排除标准

  • 1.History of spinal surgery 2.History of cancer 3.Fracture in the spine or pelvis 4.All red flags of needling 5.History of spinal canal stenosis 6.Pain that scored higher than 8 on the NPRS scale 7.Open wounds, skin diseases and hypersensitivity to metals 8.Pregnancy 9.Varicose veins 10.Subjects suffering from needle phobia 11.The participants with any coagulation disorder, the participants receiving anticoagulant therapy for any reason due to a potentially increased risk of hematoma following needling.

结局指标

主要结局

1.Numeric pain rating scale

时间窗: All the outcome measures will be measured pre (Day 1 intervention) and post (Day 5 intervention)

2.Modified Oswestry disability questionnaire

时间窗: All the outcome measures will be measured pre (Day 1 intervention) and post (Day 5 intervention)

3.Modified Modified schobers test

时间窗: All the outcome measures will be measured pre (Day 1 intervention) and post (Day 5 intervention)

次要结局

未报告次要终点

研究者

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

Dr Santosh Metgud

KAHER Institute of Physiotherapy

研究点 (1)

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