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Evaluation of Toothbrush Bristles in Plaque Reduction

Not Applicable
Completed
Conditions
Plaque, Dental
Gingivitis
Interventions
Device: Tapered bristles A
Device: Tapered bristles B
Device: End rounded bristles
Registration Number
NCT04681885
Lead Sponsor
Sunstar Americas
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
10
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Tapered bristles ATapered bristles B-
Tapered bristles AEnd rounded bristles-
Tapered bristles BTapered bristles A-
Tapered bristles BTapered bristles B-
End rounded bristlesTapered bristles A-
End rounded bristlesEnd rounded bristles-
Tapered bristles BEnd rounded bristles-
End rounded bristlesTapered bristles B-
Tapered bristles ATapered bristles A-
Primary Outcome Measures
NameTimeMethod
Change of Navy Plaque Index (Navy Pl) After One-time BrushingPre-intervention at baseline and after one-time brushing for 2 minutes at baseline

Change of Navy Plaque Index (Navy Pl) after one-time brushing in a whole mouth. The Navy Plaque Index (PI) can be either 0 (plaque is not present) or 1 (plaque is present). Each tooth is partitioned into 9 areas, and the PI is evaluated for teeth numbered 2-15 and 18-31, totaling 28 teeth. Both buccal (B) and lingual (L) sides of each tooth are assessed. The PI value of each person ranges from 0 to 504 (28 teeth × 9 areas × 2 sides). Baseline value is calculated by averaging PI values of 10 subjects before brushing. Post-brushing value is calculated by averaging PI values of 10 subjects after a one-time brushing for 2 minutes

Change of Digitally Measured Interdental Plaque Area After One-time BrushingPre-intervention at baseline and after one-time brushing for 2 minutes at baseline

Change of digitally measured interdental plaque area on non-molar teeth, facial/buccal aspect after one-time brushing by image analysis.

Secondary Outcome Measures
NameTimeMethod
Change of Navy Plaque Index (Navy PI) After 7-day BrushingPre-intervention at baseline and after 7- day brushing at baseline

Change of Navy Plaque Index (Navy Pl) after 7-day brushing in a whole mouth. The Navy Plaque Index (PI) can be either 0 (plaque is not present) or 1 (plaque is present). Each tooth is partitioned into 9 areas, and the PI is evaluated for teeth numbered 2-15 and 18-31, totaling 28 teeth. Both buccal (B) and lingual (L) sides of each tooth are assessed. The PI value of each person ranges from 0 to 504 (28 teeth × 9 areas × 2 sides). Baseline value is calculated by averaging PI values of 10 subjects before brushing. 7-day value is calculated by averaging PI values of 10 subjects after 7-day brushing.

Change of Digitally Measured Interdental Plaque Area After 7-day BrushingPre-intervention at baseline and after 7-day brushing at baseline

Change of digitally measured interdental plaque area on non-molar teeth, facial/buccal aspect after 7- day brushing by image analysis.

Trial Locations

Locations (1)

The University of Tennessee Health Science Center

🇺🇸

Memphis, Tennessee, United States

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