# Effect of immediate photobiomodulation on pain and inflammation after oral biopsy: A randomized clinical study

**Authors:** Yolanda Collado-Murcia, Francisco Parra-Perez, Pia López-Jornet

PMC · DOI: 10.1007/s00784-026-06791-1 · Clinical Oral Investigations · 2026-02-24

## TL;DR

This study found that a single session of photobiomodulation after an oral biopsy did not reduce pain or inflammation more than a sham treatment over 7 days.

## Contribution

The study provides new evidence that immediate PBM may not offer clinical benefits for post-biopsy pain or inflammation.

## Key findings

- No significant differences in pain reduction were observed between PBM and sham groups.
- Inflammation levels also showed no significant difference between the two groups.
- Both groups experienced reduced pain and inflammation over time, but not due to PBM.

## Abstract

To evaluate whether photobiomodulation (PBM) reduces postoperative pain and inflammation in patients undergoing a soft tissue oral biopsy, compared with a sham treatment.

A prospective, randomized controlled clinical study was conducted. Oral mucosal biopsies were performed using a standardized protocol. Group allocation was carried out using simple randomization. Participants were assigned to two groups: active PBM (n = 31) and simulated (sham) PBM (n = 31). A single intraoral PBM session (wavelength 940 nm, output power 0.5 W) was applied immediately after the biopsy procedure.

No statistically significant differences were observed between the groups with respect to pain or inflammation reduction during the 7-day follow-up period. Both variables decreased over time in both groups, with no significant group effect or group–time interaction effect (p = 0.279 and p = 0.220, respectively).

A single session of PBM applied immediately after a soft tissue oral biopsy did not demonstrate additional benefits compared with sham treatment in reducing postoperative pain or inflammation over a 7-day period. Further studies using optimized PBM protocols are needed to better define its potential role in this clinical setting.

## Full-text entities

- **Diseases:** burning mouth syndrome (MESH:D002054), temporomandibular joint disorders (MESH:D013705), systemic diseases (MESH:D034721), oral lesions (MESH:D009059), bleeding (MESH:D006470), tumorous lesions in the oral cavity (MESH:D009062), trismus (MESH:D014313), mental disorders (MESH:D001523), Postoperative pain (MESH:D010149), cancer (MESH:D009369), Sjogren syndrome (MESH:D012859), edema (MESH:D004487), Dental Anxiety (MESH:D001007), tissue trauma (MESH:D014947), nerve complications (MESH:D008107), Inflammation (MESH:D007249), hematoma (MESH:D006406), Pain (MESH:D010146), dehiscence (MESH:D013529), amyloidosis (MESH:D000686), mucositis (MESH:D052016), chronic pain (MESH:D059350), infection (MESH:D007239), oral mucositis (MESH:D013280)
- **Chemicals:** alcohol (MESH:D000438), OHIP14 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932344/full.md

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Source: https://tomesphere.com/paper/PMC12932344