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Effect of Night Guard Use on Masseter Muscle Thickness in Children With Bruxism

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Summary

This clinical trial registration describes a prospective study (NCT07548502) evaluating the clinical findings of bruxism and masseter muscle thickness in children aged 10-12 years using ultrasonography, and assessing the effects of night guard (occlusal splint) use on these parameters over time. The study enrolls pediatric participants with sleep-related bruxism as the condition of interest. This entry serves as an informational registry record for the proposed research and does not impose any compliance obligations.

“This prospective study aims to evaluate the clinical findings of bruxism and masseter muscle thickness in children aged 10-12 years using ultrasonography, and to assess the effects of night guard use on these parameters over time.”

NIH , verbatim from source
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About this source

ClinicalTrials.gov is the NIH-run registry of every clinical trial conducted in the United States, plus most international trials sponsored by US-based companies or institutions. By federal law, sponsors must register Phase 2 through Phase 4 studies before enrolling patients and post results within a year of completion. This feed tracks every new trial registration and study update, around 700 a month: drug interventions, device studies, behavioral protocols, observational research. Watch this if you scout drug candidates moving into mid or late-stage development, monitor competitor pipelines, or follow rare disease research where new trials signal patient hope. GovPing parses sponsor, phase, intervention, and target indication on each entry.

What changed

This ClinicalTrials.gov registration entry documents a new prospective study on the effect of night guard (occlusal splint) use on masseter muscle thickness in children aged 10-12 years diagnosed with bruxism. The study uses ultrasonography to measure clinical findings and assess changes over time with the occlusal intervention. No compliance or regulatory obligations are created by this registration entry.

Affected parties include pediatric dental and sleep researchers, clinical investigators, and healthcare providers specializing in pediatric bruxism. This study registration may inform future clinical practice guidelines and contribute to evidence-based treatment protocols for occlusal splints in pediatric patients.

Archived snapshot

Apr 23, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← ClinicalTrials.gov Studies

Effect of Night Guard Use on Masseter Muscle Thickness in Children With Bruxism

N/A NCT07548502 Kind: NA Apr 23, 2026

Abstract

This prospective study aims to evaluate the clinical findings of bruxism and masseter muscle thickness in children aged 10-12 years using ultrasonography, and to assess the effects of night guard use on these parameters over time.

Conditions: Bruxism, Bruxism, Sleep-Related

Interventions: Occlusal Splint (Night Guard)

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Last updated

Classification

Agency
NIH
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor

Who this affects

Applies to
Healthcare providers Clinical investigators Patients
Industry sector
6211 Healthcare Providers
Activity scope
Clinical trial registration Pediatric sleep research Occlusal splint study
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Topics
Pharmaceuticals Medical Devices

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