Randomized, double-blind study comparing percutaneous electrolysis and dry needling for the management of temporomandibular myofascial pain
Lopez-Martos et al. · Med Oral Patol Oral Cir Bucal · 2018
Evidence Level
STRONGOBJECTIVE
To compare percutaneous electrolysis (PNE) and dry needling (DDN) versus placebo for treating myofascial pain of the lateral pterygoid muscle
WHO
60 patients with myofascial pain syndrome of the temporomandibular joint for at least 6 months
DURATION
3 weekly sessions with 70-day follow-up
POINTS
Lateral pterygoid muscle - transcutaneous access to the upper and lower bellies of the muscle
🔬 Study Design
PNE
n=20
Percutaneous electrolysis with 2 mA galvanic current for 3 seconds
DDN
n=20
Deep dry needling without substances
Placebo
n=20
Superficial pressure without needle penetration
📊 Results in numbers
Reduction in pain at rest (PNE)
Reduction in pain at rest (DDN)
Improvement in mouth opening (PNE)
Improvement in mouth opening (DDN)
Adverse events
📊 Outcome Comparison
Pain at rest (0-10 scale)
Maximum mouth opening (mm)
This study showed that both percutaneous electrolysis and dry needling are effective treatments for temporomandibular joint (TMJ) pain. Percutaneous electrolysis, which combines needles with a small electrical current, produced faster pain improvement, while both techniques were superior to placebo treatment in reducing pain and improving mouth opening.
Article summary
Plain-language narrative summary
Myofascial pain syndrome (MPS) of the temporomandibular joint is a complex disorder that affects the masticatory muscles, causing pain and functional limitation. The lateral pterygoid muscle is frequently involved, presenting trigger points that generate local and referred pain. This randomized, double-blind, controlled study compared two minimally invasive techniques for the treatment of MPS: percutaneous electrolysis (PNE) and deep dry needling (DDN), versus a placebo procedure. Sixty patients diagnosed with MPS in the lateral pterygoid muscle, with pain for at least 6 months and limited mouth opening (<40 mm), were randomized into three groups of 20 participants each.
The PNE group received needling with application of low-intensity galvanic current (2 mA for 3 seconds), the DDN group received deep needling without introduction of substances, and the control group received superficial pressure without needle penetration. Treatments were performed once a week for three consecutive weeks, with assessments on days 28, 42, and 70 after treatment. The results demonstrated that both active techniques were significantly superior to placebo in reducing pain at rest and during mastication, as well as in improving maximum mouth opening. The PNE group showed earlier improvement, with significant pain reduction by day 28, while the DDN group presented consistent improvement throughout the follow-up period.
Pain at rest decreased from 6.0 to 1.5 in the PNE group and from 6.0 to 2.0 in the DDN group, remaining stable through day 70. Mouth opening improved from 34.5 mm to 40 mm in the PNE group and from 34 mm to 37 mm in the DDN group. TMJ functionality, assessed by a 100-point questionnaire, showed significant improvement in both active groups compared to placebo. Adverse events were minimal, with only one self-limited hematoma reported in the PNE group.
Tolerance to treatment was excellent in all groups, and the subjective evaluation of efficacy was superior in the PNE and DDN groups. The clinical implications are important, as both techniques offer safe and effective alternatives for treating temporomandibular MPS, with PNE having the advantage of faster action, possibly due to the combined effect of mechanical and electrical stimulation. The study has limitations such as the relatively small sample size, difficulty in complete blinding in invasive procedures, and exclusive focus on the lateral pterygoid muscle, when there is often involvement of multiple masticatory muscles.
Strengths
- 1Randomized, double-blind, placebo-controlled design
- 2Adequate 70-day follow-up to assess durability of effects
- 3Use of multiple validated outcome measures
- 4Standardized and validated needling technique
- 5Low rate of adverse events
Limitations
- 1Relatively small sample size for definitive conclusions
- 2Difficulty maintaining complete blinding in invasive procedures
- 3Focus only on the lateral pterygoid muscle, excluding cases with multiple affected muscles
- 4Lack of long-term follow-up
- 5Exclusion of patients with fibromyalgia or depression
Expert Commentary
Dr. Marcus Yu Bin Pai
MD, PhD · Pain Medicine · Physical Medicine and Rehabilitation · Medical Acupuncture
▸ Clinical Relevance
Temporomandibular myofascial pain with involvement of the lateral pterygoid represents one of the most refractory subtypes of temporomandibular disorders, precisely because this muscle is difficult to access and frequently underdiagnosed. Having a double-blind trial comparing percutaneous electrolysis and deep dry needling at this specific topography fills a real gap in clinical decision-making. In musculoskeletal pain practice, these patients arrive after dentists and other specialists have exhausted occlusal splints, anti-inflammatory drugs, and conventional physical therapy. The data show that both techniques produce clinically significant pain reduction—from 6.0 to 1.5 or 2.0—and measurable functional gain in mouth opening, maintained through week ten. This positions structured needling as a concrete second-line option, with an excellent safety profile evidenced by the only adverse event recorded, a self-limited hematoma in the entire PNE group.
▸ Notable Findings
The most striking finding is not the efficacy itself—expected for both active techniques—but the differential speed of response. The group undergoing percutaneous electrolysis demonstrated significant reduction by the day-28 assessment, while deep dry needling reached comparable levels more gradually throughout follow-up. This temporal pattern suggests distinct mechanisms: low-intensity galvanic current possibly amplifies the neurophysiological effect of mechanical stimulation on the trigger point, accelerating central inhibition and resolution of focal spasm. The gain in mouth opening is equally expressive—5.5 mm in the PNE group versus 3 mm in the DDN group—with direct functional relevance for mastication, speech, and quality of life. The stability of results through day 70 with only three weekly sessions reinforces the durability of the effect, which is precisely the most questioned point in this line of treatment.
▸ From My Experience
In my practice with orofacial pain and temporomandibular dysfunction, the lateral pterygoid is the muscle that most frequently surprises negatively when not identified as the primary generator of the condition. I typically see perceptible clinical response after the second session of deep dry needling in this region, and generally three to five sessions are sufficient to consolidate functional gain in mouth opening. What stands out in this article is that PNE anticipates this response to the first post-treatment evaluation—which, in practical terms, means a smaller window of frustration for the patient and better adherence to the program. At the Pain Center, we systematically combine needling with mandibular kinesiotherapy and, in cases with masseteric hyperactivity component, with short-acting muscle relaxants. The profile that responds best to needling alone, in my experience, is the patient without a marked central component—without associated fibromyalgia, without established central sensitization—exactly the profile selected in this study.
Full original article
Read the full scientific study
Med Oral Patol Oral Cir Bucal · 2018
DOI: 10.4317/medoral.22488
Access original articleScientific Review

Marcus Yu Bin Pai, MD, PhD
CRM-SP: 158074 | RQE: 65523 · 65524 · 655241
PhD in Health Sciences, University of São Paulo. Board-certified in Pain Medicine, Physical Medicine and Rehabilitation, and Medical Acupuncture. Scientific review and curation of every entry in this library.
Learn more about the author →Medical disclaimer: This content is for educational purposes only and does not replace consultation, diagnosis, or treatment by a qualified professional. Some information may be assisted by artificial intelligence and is subject to inaccuracies. Always consult a physician.
Content reviewed by the medical team at CEIMEC — Integrated Centre for Chinese Medicine Studies, a reference in Medical Acupuncture for over 30 years.
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