Efficacy of Plaque Removal of a Novel Brushing Device

Dental Plaque Clinical Trial

Official title:

Efficacy of Plaque Removal of a Novel Brushing Device Compared to a Manual Toothbrush

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05038293
• Other study ID #: STUDY00013154
• Status: Completed
• Phase: N/A
• Start date: September 17, 2021
• Est. completion date: February 1, 2022

Study information

• Verified date: March 2023
• Source: University of Washington
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this research study is to compare how a novel, automated mouthpiece-based toothbrushing device removes dental plaque compared to a manual toothbrush.

Description:

Plaque is one of the main etiological factors in dental decay and the principal etiological factor for periodontal diseases. Although toothbrushes have greatly evolved, dexterity is still the key component to an efficient cleaning routine. The primary goal is to examine 60 participants to determine the efficacy of a new powered teeth cleaning device designed to bypass the variability of individual dexterity compared with manual toothbrushing. This is a single-blind, randomized controlled trial. Sixty pediatric patients will be recruited for the study and randomized into treatment and control groups, subdivided into primary (20), mixed (20), and permanent dentition (20). Participants will be asked to abstain from brushing, flossing, gum or mouthwash use for 24 hours prior to the study visit. Plaque will be assessed using the Turesky Modification of the Quigley-Hein Plaque Index before and after a one-time brushing with the assigned study device. A soft tissue assessment will be conducted and intraoral photos taken pre- and post-brushing.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 42
• Est. completion date: February 1, 2022
• Est. primary completion date: February 1, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 5 Years to 17 Years

Eligibility

Inclusion Criteria:

• Between the ages of 5-17
• In good general health
• Fluent in English
• Parent or guardian willing and able to provide written informed consent
• Have 16 scorable teeth (non-crown/bridge/or full amalgams)
• Have had a dental cleaning and exam in the past 24 months

Exclusion Criteria:

• Advanced periodontal disease or severe gum disease
• Mouth or teeth pain that prevents brushing in any areas
• Intraoral piercings (tongue or lip) that cannot be removed
• Non-controlled diabetes
• Any autoimmune or infectious disease or any medical condition that would delay wound healing
• Untreated visible cavities or untreated dental work
• Oral or gum surgery in the previous 2 months
• Take antibiotic premedication for dental procedures
• Undergoing or require extensive dental or orthodontic treatment
• Current smoker
• Generalized recession over 1mm

Related Conditions & MeSH terms

• Dental Plaque

Intervention

Device:
• Automated mouthpiece-based toothbrush
One-time use during study visit.
• Manual toothbrush
One-time use during study visit.

Locations

Country	Name	City	State
United States	University of Washington, School of Dentistry, Regional Clinical Dental Research Center (RCDRC)	Seattle	Washington

Sponsors (1)

Lead Sponsor	Collaborator
University of Washington

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change From Baseline in Dental Plaque Removal Efficacy Using Turesky Modification of the Quigley-Hein Plaque Index	Average Change from baseline plaque index after brushing with the automated mouthpiece-based brushing device versus a manual toothbrush. The Turesky Modification of the Quigley-Hein Plaque Index evaluates 6 areas per tooth and gives a score from 0-5 with 0 being no plaque and 5 being the highest amount of plaque and the average score for all sites was used for analysis.	baseline,1 minute after brushing
Secondary	Change From Baseline in Presence of Soft Tissue Abrasion After Use of Automated Mouthpiece-based Brushing Versus Manual Toothbrush	Number of participants with soft tissue abrasion after brushing with the automated mouthpiece-based.brushing device versus a manual toothbrush. An intraoral soft tissue examination will be done before and after brushing and a binary scale will be used to note any areas of abrasion (yes or no). Outcome is the presence of any soft tissue abrasion that was not present prior to brushing.	baseline, 1 minute after brushing