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Effectiveness of Autobrush® Versus Manual Toothbrush Among Adolescents With Fixed Orthodontic Appliances

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Summary

NIH ClinicalTrials.gov registered a randomized crossover clinical trial (NCT07537790) comparing the effectiveness of Autobrush® U-shaped automatic toothbrush versus conventional manual toothbrush in reducing dental plaque among adolescents aged 12-15 with fixed orthodontic appliances. The study will measure Full Mouth Plaque Score (FMPS) as the primary outcome and is being conducted at KAUD in Saudi Arabia.

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What changed

NIH registered a new clinical trial (NCT07537790) on ClinicalTrials.gov. The study is a randomized crossover clinical trial comparing U-shaped automatic toothbrush (Autobrush®) versus manual toothbrush using Bass technique for reducing dental plaque in adolescents with fixed orthodontic appliances. Participants aged 12-15 will undergo both interventions with a 2-week washout period.

Healthcare providers and clinical investigators involved in orthodontic research should note this as a registration of ongoing research in oral hygiene assessment. The study uses Full Mouth Plaque Score (FMPS) as the primary outcome measure and is scheduled for completion April 17, 2026.

Archived snapshot

Apr 18, 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.

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Effectiveness of Autobrush® Versus Manual Toothbrush Among Adolescents With Fixed Orthodontic Appliances

N/A NCT07537790 Kind: NA Apr 17, 2026

Abstract

This study is a randomized crossover clinical trial designed to compare the effectiveness of a U-shaped automatic toothbrush (Autobrush®) versus a conventional manual toothbrush in reducing dental plaque among adolescents undergoing fixed orthodontic treatment. Each participant will be exposed to both interventions during the study period due to the crossover design.

The inclusion criteria included healthy adolescents aged 12-15 years, whom were undergoing treatment with fixed orthodontic appliances attending the Orthodontic Department at KAUD Medically compromised adolescents, those with disabilities, individuals without fixed orthodontic appliances, and adolescents with known nylon allergies were excluded.

Before appointment, participants were instructed to refrain from all oral hygiene measures (e.g., brushing, chewing gum) for 12 hours. On the appointment time, at the clinic, participants are assigned randomly to a toothbrush group and given disclosing solution to visualize plaque.

The FMPS was recorded before brushing. Then, participants brush under supervision with their assigned toothbrush group, either manual toothbrush using Bass technique for 2 minutes or using Autobrush® with side-to-side motion for 30 seconds. After brushing, FMPS is reassessed using the same disclosing procedure. Following a washout period of at least 2 weeks, the participant repeats the procedure with the alternative toothbrush.

Conditions: Full Mouth Plaque Score (FMPS)

Interventions: U-shaped toothbrush (Autobrush®), Manual regular toothbrush

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Last updated

Classification

Agency
NIH
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
NCT07537790

Who this affects

Applies to
Healthcare providers Clinical investigators
Industry sector
3345 Medical Device Manufacturing
Activity scope
Clinical trial registration Dental device research Oral hygiene assessment
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Topics
Clinical Research Medical Devices Public Health

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