# Effectiveness of laser photobiomodulation in the management of trigeminal neuralgia: a systematic review and meta-analysis

**Authors:** Paula da Costa Taddeucci, Gabriel Campos Louzeiro, Karen Cherubini, Juliana Cassol Spanemberg, Fernanda Gonçalves Salum

PMC · DOI: 10.1007/s10103-026-04804-9 · Lasers in Medical Science · 2026-02-03

## TL;DR

This study reviews clinical trials to evaluate laser therapy's effectiveness in reducing pain for trigeminal neuralgia patients.

## Contribution

A systematic review and meta-analysis showing laser photobiomodulation as a promising adjuvant therapy for trigeminal neuralgia.

## Key findings

- Eight out of nine studies showed significant pain reduction with laser therapy compared to controls.
- Meta-analysis found a significant effect of laser therapy in reducing pain scores.
- High heterogeneity and lack of standardized protocols limit definitive conclusions.

## Abstract

This systematic literature review aimed to assess the effectiveness of laser photobiomodulation therapy (PBM) in reducing pain in patients with trigeminal neuralgia and postherpetic neuralgia. Randomized controlled clinical trials were identified through searches in the following databases: PubMed, Web of Science, LILACS, EMBASE, Scopus, and the Cochrane Library. No studies involving patients with postherpetic neuralgia met the inclusion criteria and were therefore excluded. Nine studies, comprising a total of 387 patients diagnosed with trigeminal neuralgia, were included. In seven of these studies, patients also received pharmacological treatment, which was initiated either prior to or concurrently with the PBM intervention. A sham laser was used as a control in six studies. PBM parameters varied widely and were often incompletely reported, limiting the ability to compare treatment protocols. Qualitative analysis showed that eight out of nine studies reported a significantly greater reduction in pain scores in the PBM groups compared to control groups. A low to moderate risk of bias was found in two-thirds of the studies. The meta-analysis, which included five studies, demonstrated a significant effect of PBM in reducing pain scores (MD − 2.17; 95% CI, − 3.30 to − 1.04; P = 0.0002), although high heterogeneity was observed (I² = 92%). PBM appears to be an effective adjuvant therapy for trigeminal neuralgia, with a favorable safety profile and potential to reduce medication dependency. Nevertheless, the results should be interpreted cautiously due to substantial heterogeneity, lack of PBM protocol standardization, and limited long-term outcome data.

The online version contains supplementary material available at 10.1007/s10103-026-04804-9.

## Linked entities

- **Diseases:** trigeminal neuralgia (MONDO:0008599), postherpetic neuralgia (MONDO:0041052)

## Full-text entities

- **Diseases:** paralysis (MESH:D010243), infection (MESH:D007239), trigeminal ganglion block (MESH:D045888), Headache Disorders (MESH:D020773), vomiting (MESH:D014839), blood dyscrasias (MESH:D006402), neuropathies (MESH:D009422), muscle spasm (MESH:D013035), tumors (MESH:D009369), Trigeminal Neuralgia (MESH:D014277), erythema multiforme (MESH:D004892), chronic pain (MESH:D059350), angle (MESH:D009464), xerostomia (MESH:D014987), Neuropathic pain (MESH:D009437), neurological deficits (MESH:D009461), Facial Neuralgia (MESH:D005156), Headache (MESH:D006261), PBM (MESH:D016609), nausea (MESH:D009325), Facial Pain (MESH:D005157), Postherpetic Neuralgia (MESH:D051474), allodynia (MESH:D006930), vascular malformations (MESH:D054079), impairment of orofacial functions (MESH:D003072), cutaneous lesions (MESH:D009059), Pain (MESH:D010146), herpes zoster (MESH:D006562), multiple sclerosis (MESH:D009103), arteriovenous malformations (MESH:D001165), vascular (MESH:D057772), inflammation (MESH:D007249), paresthesia (MESH:D010292), acute painVitamin (MESH:D000208)
- **Chemicals:** Vitamin B12 (MESH:D014805), methylprednisolone (MESH:D008775), Benfotiamine (MESH:C013835), bupivacaine (MESH:D002045), gliclazide (MESH:D005907), Nefopam hydrochloride (MESH:D009340), NANTCL (-), metformin (MESH:D008687), Vitamin B6 (MESH:D025101), glibenclamide (MESH:D005905), baclofen (MESH:D001418), Carbamazepine (MESH:D002220), gabapentin (MESH:D000077206), oxcarbazepine (MESH:D000078330), ATP (MESH:D000255), CO2 (MESH:D002245)
- **Species:** Meleagris gallopavo (common turkey, species) [taxon 9103], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12864350/full.md

## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC12864350/full.md

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Source: https://tomesphere.com/paper/PMC12864350