# Assessment of photobiomodulation combined with new restorative material for teeth with molar incisor hypomineralization on control of hypersensitivity and longevity of restorations: Protocol for a randomized controlled blind clinical trial

## TL;DR

This study will test if combining photobiomodulation with a new dental material helps reduce tooth sensitivity and improve restoration longevity in children with MIH.

## Contribution

The study introduces a novel combination of photobiomodulation and a self-cure resin for treating MIH-related hypersensitivity.

## Key findings

- Photobiomodulation combined with self-cure resin may reduce hypersensitivity in MIH-affected molars.
- The clinical performance of the self-cure resin will be evaluated for restoration longevity.
- Comparisons will be made between three treatment approaches for controlling hypersensitivity over time.

## Abstract

Molar incisor hypomineralization (MIH) is a qualitative defect of enamel development that occurs in the mineralization phase. MIH affects one or more permanent molars and, occasionally, permanent incisors. The aim of the proposed study is to determine whether photobiomodulation combined with a new self-cure resin improves hypersensitivity in molars with MIH (primary outcome). Secondary outcomes include assessing the clinical performance of the self-cure composite resin in terms of restoration longevity and comparing the effectiveness of three interventions—photobiomodulation combined with self-cure resin, self-cure resin alone, and photobiomodulation combined with bulkfill photopolymerizable resin—in controlling hypersensitivity over time. Permanent molars with MIH in patients 6–10 years of age will be allocated to three groups. Group 1: photobiomodulation + self-cure composite resin restoration; Group 2: self-cure composite resin restoration; Group 3: photobiomodulation + restoration in bulk-fill photopolymerizable composite resin. Photobiomodulation will be performed in a single session involving low-level laser administered to four different points. The laser will be used at a wavelength of 808 nm, power of 100 mW and energy of 1 J per points; irradiance will be 3571 mW/cm2, with a total radiant exposure of 35.7 J/cm2. Data normality will be checked using the Shapiro-Wilk test, and variance homogeneity will be assessed with the Levene test. Descriptive statistics will be used to present the data, with continuous variables expressed as mean and standard deviation, and categorical variables by relative frequency. To compare the Wong-Baker Faces Pain Rating Scale and SCASS scales, repeated measures ANOVA will be employed, considering the 3 groups and 5 time points. Bonferroni adjustment will be applied for post-hoc comparisons. Sphericity will be tested with Mauchly’s test, and if violated, Greenhouse-Geisser correction will be applied. A significance level of 0.05 will be adopted.

ClinicalTrials.gov NCT06538142