Evaluation of Toothbrush Bristles in Plaque Reduction

Gingivitis Clinical Trial

Official title:

Evaluation of Toothbrush Bristles in Plaque Reduction

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04681885
• Other study ID #: CLP-2020-06-01-1
• Status: Completed
• Phase: N/A
• Start date: June 30, 2021
• Est. completion date: September 17, 2021

Study information

• Verified date: September 2021
• Source: Sunstar Americas
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this cross-over clinical research is to evaluate the cleaning efficacy of toothbrushes tufted with two types of tapered bristles and end rounded bristles in removal of interdental plaque with clinical measurement (Plaque Index) and objective measurement (digitally measured plaque area). This study will demonstrate the influence by a type of processing bristles on removal of interdental plaque and determine an agreement between the different evaluation methods.

This is a randomized evaluator-masked crossover study with 10 subjects. Subjects will be randomly allocated to three test groups. Subjects will use the assigned toothbrush at baseline appointment and two times a day for a week. Plaque Index and plaque area will be assessed before/after one time use at baseline and Day 7. Subjects will be assigned to another toothbrush after one week wash-out period.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: September 17, 2021
• Est. primary completion date: September 17, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria: Individuals may be included in the study if they meet all of the following inclusion criteria:

• Must have read, understood and signed an informed consent prior to being entered into the study

• Must be 18 to 70 years of age, male or female

• Have at least 20 natural or restored teeth

• Must have average Plaque Index of Ramfjord teeth at baseline greater than 2(Quigley and Hein) at screening

• Agree not to have a dental prophylaxis or any other elective, non-emergency dental procedures (other than those provided during the study) any time during the study

• Agree to refrain from regular oral hygiene regimen for 24 hours and eating for 4 hours before the appointment in the study

• Agree to abstain from the use of any dental products other than those provided in the study

• Agree to comply with the conditions and schedule of the study

Exclusion Criteria: Individuals are not eligible for participation in this study if any of the following are noted:

• Physical limitations or restrictions that might preclude normal tooth brushing

• Evidence of gross oral pathology

• Presence of severe gingivitis with 30 or more sites showing bleeding on probing

• Evidence of major soft tissue lesions or trauma at the baseline visit as determined by the Investigator/Examiner

• Chronic disease with concomitant oral manifestations

• Subjects who are currently undergoing, or require, extensive dental work, orthodontic treatment or periodontal surgery or orthodontic treatment in the preceding 3 months

• Currently using bleaching trays

• Eating disorders

• Recent history of substance abuse

• Smoking >10 cigarettes/day

• Participation in other clinical studies within 14 days of screening

Related Conditions & MeSH terms

• Dental Plaque
• Gingivitis
• Plaque, Dental

Intervention

Device:
• Tapered bristles A
Subjects use the toothbrush two times daily with a fluoride toothpaste for 2 minutes with instructed brushing method for one week .
• Tapered bristles B
Subjects use the toothbrush two times daily with a fluoride toothpaste for 2 minutes with instructed brushing method for one week.
• End rounded bristles
Subjects use the toothbrush two times daily with a fluoride toothpaste for 2 minutes with instructed brushing method for one week.

Locations

Country	Name	City	State
United States	The University of Tennessee Health Science Center	Memphis	Tennessee

Sponsors (1)

Lead Sponsor	Collaborator
Sunstar Americas

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change of plaque index after one-time brushing	Change of plaque index (Navy Pl) for interdental area after one-time brushing in a whole mouth.	Baseline
Primary	Change of plaque area after one-time brushing	Change of digitally measured interdental plaque area on non-molar teeth after one-time brushing by image analysis.	Baseline
Secondary	Change of plaque index at 7 days	Change of plaque index (Navy PI) for interdental area in a whole mouth at 7 days of test product use.	Baseline, 7 days
Secondary	Change of plaque area at 7 days	Change of digitally measured interdental plaque area on non-molar teeth at 7 days of test product use .	Baseline, 7 days