Efficacy of Different Toothbrushes and Hygiene Regimen
Primary Purpose
Dental Plaque, Halitosis
Status
Unknown status
Phase
Phase 1
Locations
Brazil
Study Type
Interventional
Intervention
Total 12 regimen
Toothbrushing alone
Sponsored by
About this trial
This is an interventional prevention trial for Dental Plaque
Eligibility Criteria
Inclusion Criteria:
- Good general health;
- Age 12 to 17;
- Absence of motor, comprehension and cognitive difficulties that impede adequate oral hygiene.
Exclusion Criteria:
- Active dental caries with cavity exposing dentin (visible cavity) on teeth for which the simplified oral hygiene index will be used. If these teeth are not present, adjacent teeth may be considered;
- Teeth with formation defects and dental crowding;
- Periodontal disease (tooth mobility > 2 mm, pocket > 5 mm, gingivitis);
- Parafunctional habits (bruxism, nail biting), active clamps for removable partial dentures, use of orthodontic appliance;
- Volunteer or legal guardian who does not agree with the terms of the study or has difficulty appearing for the follow up appointments;
- Pregnant volunteers;
- Use of medications that alter gingival health, such as antibiotics, in the previous three months;
- Use of mouthwash or toothpaste containing products for the control of biofilm;
- Smokers;
- Systemic disease (diabetes).
Sites / Locations
- Universidade Metropolitana de Santos
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Total 12 regimen group
Tooth brushing alone group
Arm Description
This group will use the following procedure: Colgate Ultrasoft toothbrush, Colgate Total 12 toothpaste and Plax Mouthwash.
This group will use Colgate Ultrasoft toothbrush and Colgate Cavity Protection toothpaste.
Outcomes
Primary Outcome Measures
Evaluation of change in biofilm index
The gingival health assessments will be performed through a visual examination for the determination of the visible plaque index, gingival bleeding and oral health at baseline as well as after the use of brush.
Secondary Outcome Measures
Change in halitosis index
Halitosis index using the portable BreathAlert™ sulfide monitor (Tanita Corporation, Japan).
Full Information
NCT ID
NCT04216069
First Posted
December 18, 2019
Last Updated
September 17, 2020
Sponsor
University of Nove de Julho
1. Study Identification
Unique Protocol Identification Number
NCT04216069
Brief Title
Efficacy of Different Toothbrushes and Hygiene Regimen
Official Title
Evaluation of the Efficacy of a Commercially Available Regimen Versus Brushing Alone on Established Plaque and Gingivitis on Adolescents: Study Protocol for a Randomized, Controlled, Blind Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
September 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 5, 2021 (Anticipated)
Primary Completion Date
June 30, 2021 (Anticipated)
Study Completion Date
December 25, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Nove de Julho
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
To evaluate: 1) Evaluate the efficacy of a regimen commercially available versus brush alone on established plaque and gingivitis on adolescents. The Group 1 will use the following procedure: Colgate Ultrasoft toothbrush, Colgate Total 12 toothpaste and Plax Mouthwash, and the other Group will use Colgate Ultrasoft toothbrush and Colgate Cavity Protection toothpaste; 2) The level of halitosis. Two calibrated and blinded examiners (Cohen Kappa 85%) will evaluate the gingival condition using the visible plaque indices, a simplified oral hygiene index - IHOS and gingival bleeding index, with the aid of a WHO probe. For the evaluation of halitosis levels, all individuals will respond to a questionnaire regarding personal data, general and oral health, which includes hygiene habits and received previous guidelines for the procedures to be performed in the second moment. At the next consultation, subjects will be assessed clinically for halitosis using the portable BreathAlert™ sulfide monitor (Tanita Corporation, Japan), in addition to the evaluation of the tongue flap index (ISL), pH and salivary flow. The evaluations will be in the following periods: baseline, 1, 3 and 6 months of brushing. Data will be submitted to descriptive statistical analysis to demonstrate the distributions frequency of biofilm indices and gingival bleeding. The differences in the criteria evaluated will be submitted to Fisher's exact test (α = 0.05) and their performance at different times will be evaluated by the Mann-Whitney test (α = 0.05).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dental Plaque, Halitosis
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
The outcome assessor will not know to which group the participant belongs.
Allocation
Randomized
Enrollment
58 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Total 12 regimen group
Arm Type
Experimental
Arm Description
This group will use the following procedure: Colgate Ultrasoft toothbrush, Colgate Total 12 toothpaste and Plax Mouthwash.
Arm Title
Tooth brushing alone group
Arm Type
Experimental
Arm Description
This group will use Colgate Ultrasoft toothbrush and Colgate Cavity Protection toothpaste.
Intervention Type
Other
Intervention Name(s)
Total 12 regimen
Intervention Description
The volunteers will be invited with their caregivers to a lecture administered with the aim of clarifying the importance of oral hygiene and motivating brushing among the volunteers. Written clarifications will also be given in the form of an illustrative pamphlet. The volunteers will be trained in the technique through supervised brushing in front of a mirror. Subjects from the Group 1 will use a regimen with Colgate Total 12 toothpaste + Plax mouthwash + Colgate Ultrasoft toothbrush. Subjects will be instructed to use only their assigned group during the study period. The treatment products will be re-supplied at regular intervals. Subjects will return with their assigned products to the study site before receiving new products.
There will be no restrictions regarding diet habits during the course of the study. Upon completion of the study, subjects will be instructed to return all used and used products.
Intervention Type
Other
Intervention Name(s)
Toothbrushing alone
Intervention Description
The volunteers will be invited with their caregivers to a lecture administered with the aim of clarifying the importance of oral hygiene and motivating brushing among the volunteers. Written clarifications will also be given in the form of an illustrative pamphlet. The volunteers will be trained in the technique through supervised brushing in front of a mirror. Group 2 will use Colgate Cavity Protection Toothpaste + Colgate Ultrasoft toothbrush. Subjects will be instructed to use only their assigned group during the study period. The treatment products will be re-supplied at regular intervals. Subjects will return with their assigned products to the study site before receiving new products.
There will be no restrictions regarding diet habits during the course of the study. Upon completion of the study, subjects will be instructed to return all used and used products.
Primary Outcome Measure Information:
Title
Evaluation of change in biofilm index
Description
The gingival health assessments will be performed through a visual examination for the determination of the visible plaque index, gingival bleeding and oral health at baseline as well as after the use of brush.
Time Frame
Baseline, after 1, 3 and 6 months of toothbrushing.
Secondary Outcome Measure Information:
Title
Change in halitosis index
Description
Halitosis index using the portable BreathAlert™ sulfide monitor (Tanita Corporation, Japan).
Time Frame
Baseline, after 1, 3 and 6 months of toothbrushing.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Good general health;
Age 12 to 17;
Absence of motor, comprehension and cognitive difficulties that impede adequate oral hygiene.
Exclusion Criteria:
Active dental caries with cavity exposing dentin (visible cavity) on teeth for which the simplified oral hygiene index will be used. If these teeth are not present, adjacent teeth may be considered;
Teeth with formation defects and dental crowding;
Periodontal disease (tooth mobility > 2 mm, pocket > 5 mm, gingivitis);
Parafunctional habits (bruxism, nail biting), active clamps for removable partial dentures, use of orthodontic appliance;
Volunteer or legal guardian who does not agree with the terms of the study or has difficulty appearing for the follow up appointments;
Pregnant volunteers;
Use of medications that alter gingival health, such as antibiotics, in the previous three months;
Use of mouthwash or toothpaste containing products for the control of biofilm;
Smokers;
Systemic disease (diabetes).
Facility Information:
Facility Name
Universidade Metropolitana de Santos
City
Santos
State/Province
SP
ZIP/Postal Code
11045-401
Country
Brazil
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Caroline M Moriyama, PhD
Phone
+55 13 32283400
Email
caroline.cmm@hotmail.com
12. IPD Sharing Statement
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Efficacy of Different Toothbrushes and Hygiene Regimen
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