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Completed Not applicable Interventional Accepts healthy volunteers

Comparion of Effects of Two Different Power Toothbrushes on Plaque and Gum Health

ClinicalTrials.gov ID: NCT07813546

Public ClinicalTrials.gov record NCT07813546. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 16, 2026, 10:49 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Six-Week Randomized, Parallel Design Study to Compare the Effects of Philips Sonicare 9900 Prestige Versus an Oscillating-Rotating Power Toothbrush on Plaque and Gum Health

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The goal of this clinical trial is to learn if powered toothbrushing with a side-to-side motion is more effective than powered toothbrushing with oscillating-rotation motion in removing dental plaque. It will also learn about the safety of power toothbrushing with both products. The main questions the study aims to answer are: Does side-to-side power toothbrushing remove more dental plaque than oscillating-rotation toothbrushing? Does side-to-side power toothbrushing reduce symptoms of gingivitis better than oscillating-rotation toothbrushing? Participants will: Brush their teeth twice a day with either a side-to-side or oscillating-rotation power toothbrush Visit the clinic twice during the study: once at baseline and six weeks after the study starts. Keep a diary of when they brushed their teeth

Study identification

NCT ID
NCT07813546
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
295 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 59 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 23, 2021
Primary completion
Jul 27, 2021
Completion
Jul 27, 2021
Last update posted
Sep 9, 2026

2021

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Salus Research, Inc. Fort Wayne Indiana 46825

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07813546, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 9, 2026 · Synced Sep 16, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07813546 live on ClinicalTrials.gov.

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