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临床试验/NCT07637760
NCT07637760尚未招募不适用

Dry Needling or Percutaneous Electrolysis for Managing Myofascial Trigger Points? A Randomized Clinical Trial

Universidad Complutense de Madrid1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年9月15日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
试验地点
1

研究概览

简要总结

Dry needling (DN) and percutaneous electrolysis (PE) are minimally invasive physiotherapy techniques commonly used for the management of myofascial trigger points. DN consists of inserting a fine filiform needle into a hyperirritable area within a taut band of skeletal muscle, with the aim of eliciting local twitch responses and reducing myofascial pain. PE follows a similar needle-based approach but combines the mechanical stimulus of the needle with the application of a galvanic electrical current, producing an electrochemical reaction in the targeted tissue. Both techniques have been increasingly used in clinical practice for musculoskeletal pain conditions, including shoulder pain, although the evidence comparing their relative effectiveness remains limited.

Shoulder pain is one of the most prevalent musculoskeletal disorders and is frequently associated with the presence of active myofascial trigger points. Among the shoulder muscles, the infraspinatus has been identified as a clinically relevant structure because its trigger points may reproduce referred pain patterns commonly reported by patients with shoulder symptoms and may contribute to pain, reduced strength, altered mobility, and functional disability. Previous studies have suggested that invasive treatment of infraspinatus trigger points may produce short-term improvements in pain sensitivity and shoulder-related symptoms. However, most available research has examined dry needling or percutaneous electrolysis separately, and direct comparisons between both interventions in patients with shoulder pain remain scarce.

The physiological mechanisms underlying these techniques are not yet fully understood. Dry needling is thought to act through mechanical and neurophysiological mechanisms, including disruption of dysfunctional motor endplates, reduction of local nociceptive input, elicitation of local twitch responses, and activation of segmental and descending inhibitory pathways. Percutaneous electrolysis may share some of these needling-related effects, while also adding a galvanic current that may induce local biochemical changes and promote tissue recovery processes. Nevertheless, it remains unclear whether the addition of electrical current provides superior clinical effects compared with dry needling alone.

Since limited research has directly compared dry needling and percutaneous electrolysis applied to active myofascial trigger points of the infraspinatus in patients with shoulder pain, the present study aimed to compare the effectiveness of both techniques as complementary interventions to manual therapy and therapeutic exercise. Specifically, this study sought to determine whether percutaneous electrolysis or dry needling produced greater short-term improvements in pain intensity and shoulder-related disability.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Presence of shoulder pain for at least 3 months.
  • Shoulder pain intensity greater than 3 points on the visual analogue scale (VAS).
  • Shoulder-related disability greater than 20 points on the DASH questionnaire.
  • Presence of at least one active myofascial trigger point in the infraspinatus muscle.
  • Reproduction of the patient's familiar shoulder pain during palpation of the infraspinatus trigger point.
  • Ability to understand the study procedures and provide written informed consent.

排除标准

  • Previous shoulder surgery or traumatic shoulder injury in the affected region.
  • Presence of severe structural or systemic pathology affecting the shoulder region, such as fracture, tumour, infection, inflammatory disease, or neurological disorder.
  • Clinical signs suggestive of cervical radiculopathy or other neurological conditions that could explain the shoulder symptoms.
  • Use of physiotherapy treatment, invasive therapy, or analgesic/anti-inflammatory medication during the week before participation.
  • Contraindications to dry needling or percutaneous electrolysis, including needle phobia, anticoagulant therapy, bleeding disorders, pregnancy, pacemaker or implanted electrical devices, local skin infection, or altered skin sensitivity in the treatment area.

研究组 & 干预措施

Control group

Active Comparator

Combination of manual therapy, therapeutic exercise and dry needling

干预措施: Dry needling (Other)

Experimental Group - High intensity and short time electrolysis dose

Experimental

Combination of manual therapy, therapeutic exercise and percutaneous electrolysis

干预措施: Manual therapy (Other)

Experimental Group - High intensity and short time electrolysis dose

Experimental

Combination of manual therapy, therapeutic exercise and percutaneous electrolysis

干预措施: Therapeutic exercise (Behavioral)

Experimental Group - High intensity and short time electrolysis dose

Experimental

Combination of manual therapy, therapeutic exercise and percutaneous electrolysis

干预措施: Percutaneous Electrolysis (High Intensity - Short Time) (Other)

Experimental Group - Low intensity and long time electrolysis dose

Experimental

Combination of manual therapy, therapeutic exercise and percutaneous electrolysis

干预措施: Percutaneous electrolysis (Low Intensity - Long Time) (Other)

Experimental Group - Low intensity and long time electrolysis dose

Experimental

Combination of manual therapy, therapeutic exercise and percutaneous electrolysis

干预措施: Manual therapy (Other)

Experimental Group - Low intensity and long time electrolysis dose

Experimental

Combination of manual therapy, therapeutic exercise and percutaneous electrolysis

干预措施: Therapeutic exercise (Behavioral)

Control group

Active Comparator

Combination of manual therapy, therapeutic exercise and dry needling

干预措施: Manual therapy (Other)

Control group

Active Comparator

Combination of manual therapy, therapeutic exercise and dry needling

干预措施: Therapeutic exercise (Behavioral)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

JUAN ANTONIO VALERA CALERO

Principal Investigator

Universidad Complutense de Madrid

研究点 (1)

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