跳至主要内容
临床试验/CTRI/2025/07/091668
CTRI/2025/07/091668招募中2 期

Electroacupuncture for Low back pain. A comparative study of local versus distal points.

Annamalai1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年8月1日最近更新:

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
60
试验地点
1
主要终点
Visual analog scale(VAS)

研究概览

简要总结

Low back pain is a common musculoskeletal condition causing discomfort from the lower border of the 12th rib to the inferior gluteal fold, often leading to functional limitation, disability, and economic burden. It has a global prevalence of 7.10 percent and 64.8 percent in India, with only a portion of affected individuals seeking treatment. Contributing factors include obesity, poor posture, manual labor, and mental health issues. Conventional treatments involve medications like NSAIDs and opioids, which can have adverse effects. As an alternative, acupuncture and electroacupuncture are widely used for pain relief. Electroacupuncture enhances pain modulation by stimulating opioid release and brain activity in pain-related regions. According to Traditional Chinese Medicine, chronic low back pain is related to kidney deficiency, and specific acupuncture points such as UB 23, UB 25, and UB 40 are commonly used. This study aims to compare the effectiveness of electroacupuncture applied to local points UB 23 and UB 25 versus the distal point UB 40. A comparative study will be conducted with 60 participants divided into two groups, receiving treatment for 10 days. Outcomes will be measured using the Visual Analog Scale and Oswestry Disability Index to evaluate pain reduction and functional improvement.

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
18.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • The study includes adults aged 18-50 experiencing acute or subacute non-specific low back pain, encompassing both males and females who consent to participate in the research.

排除标准

  • include participants with open wounds, burns, or scalds in the specific areas, those who have undergone recent spinal surgeries, individuals with serious medical conditions such as spinal tumors or fractures, those with metal prosthetics inside the body, individuals consuming alcohol or psychotropic medications during the study period, pregnant or breast-feeding women, those participating in other clinical studies, and individuals with a needle phobia.

结局指标

主要结局

Visual analog scale(VAS)

时间窗: Baseline and after 10 days

次要结局

  • Oswestry Disability Index(Before and after 10 days of intervention.)

研究者

发起方
Annamalai
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Annamalai Dharuman

International Institute of Yoga and Naturopathy Medical Sciences

研究点 (1)

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