NCT07121933已完成不适用
An Evaluation of The Erchonia® PPL Laser as a Pre-Treatment Adjunct to Enhance Standard Erchonia Red Laser Therapy for the Temporary Relief of Nociceptive Musculoskeletal Pain
Erchonia Corporation1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2025年8月20日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 44
- 试验地点
- 1
研究概览
简要总结
This study is to see if applying pre-treatment with the Erchonia® PPL blue laser therapy, followed sequentially with the standard Erchonia red laser therapy can help reduce nociceptive musculoskeletal pain
详细描述
It is the goal of this single (active) group study to evaluate the efficacy of the pre-treatment with the Erchonia® PPL blue laser therapy, followed sequentially with the standard Erchonia red laser therapy, is non-inferior to (equivalent to or superior to) the standard Erchonia red laser therapy when applied alone in providing temporary relief of nociceptive musculoskeletal pain
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 22 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •22 years of age or older
- •Primary language is English
- •Subject presents with with one or more of:
- •chronic neck pain on the right side of the neck and/or the left side of the neck and/or the back of the neck; and/or
- •chronic shoulder pain on the right shoulder and/or the left shoulder.
- •Subject is diagnosed with of one or more of the following:
- •Osteoarthritis: Degenerative Joint Disorder (DJD)
- •Chronic Muscle Spasms
- •Cervical and Thoracic Spine Sprain Strain
- •Pain is chronic, having persisted for longer than the past 30 days
- •Self-reported Pain rating on the 0-100 Visual Analog Scale (VAS) of 50 or greater.
- •Willing and able to refrain from consuming any over-the-counter and/or prescription medication(s) and/or herbal supplements intended for the relief of pain and/or inflammation, including muscle relaxants throughout the course of study participation.
- •Willing and able to refrain from engaging in any non-study procedure therapies throughout the course of study participation, including conventional therapies such as physical therapy, occupational therapy and hot or cold packs, as well as alternative therapies such as chiropractic care and acupuncture
排除标准
- •Presenting primary pain is located outside or in addition to the region of the neck (right side/left side/back) or the shoulder (right and/or left side)
- •Etiology of neck/shoulder pain cannot be definitively diagnosed; or has bene diagnosed as being in whole or in part other than that of osteoarthritis, chronic muscle spasms or cervical and thoracic spine sprain strain; or other potentially contributing etiologies cannot be satisfactorily ruled out
- •Pain is acute: symptoms prevailed for fewer than each of the prior 30 days
- •Current active chronic pain disease: such as chronic fatigue syndrome and fibromyalgia
- •Use of analgesics or muscle relaxants within 7 days prior to study procedure administration
- •Use of systemic corticosteroid therapy (inhaled and topical corticosteroids permitted), narcotics or Botulinum toxin (Botox®) injection in the neck / shoulder region within 30 days prior to study procedure administration
- •Active cancer or treatment for cancer within the last 6 months
- •Unstable cardiac disease, such as recent cardiac arrhythmia, congestive heart failure or myocardial infarction
- •Prior surgery to the neck/shoulder region
- •Known herniated disc injury
- •Active infection, would or other external trauma to the areas to be treated with the laser
- •Medical, physical, or other contraindications for or sensitivity to light therapy
- •Serious known mental health illness such as dementia or schizophrenia; psychiatric hospitalization in the past two years
- •Pregnant or breast feeding
- •Participation in a research study within the past 30 days
研究者
研究点 (1)
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