Evaluation of 3 Oral Self-care Regimens on Clinical Signs of Inflammation and Plaque

NCT ID: NCT05766995

Last Updated: 2023-03-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 105 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-08-03
• Study Completion Date: 2021-09-03

Brief Summary

To compare three different oral hygiene regimens on changes in gum tissue appearance, gum bleeding, and plaque scores.

Detailed Description

The goal of this clinical trial was to compare the effect of different battery powered water in and adult population with mild to moderate gingivitis. The main questions it aims to answer are:

• Is there a difference between the two water flosser devices on gum bleeding scores?
• Is there a difference between the two water flosser devices on plaque accumulation and removal?
• Is there a difference between the two water flosser devices on signs of gingivitis?

Researchers will compare the two groups using a water flosser (experimental) to see how it compares to traditional brushing and flossing (control).

Conditions

Gingivitis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: DOUBLE

Study Groups

Manual toothbrush and water flosser with standard jet tip

Brush with a standard ADA manual toothbrush twice daily followed by water flossing once in the evening

Group Type: EXPERIMENTAL

Waterpik Water Flosser

Intervention Type: DEVICE

A pulsating water flosser and jet tip designed to clean between the teeth and below the gingival margin.

Manual toothbrush and water flosser with targeted jet tip

Brush with a standard ADA manual toothbrush twice daily followed by water flossing once in the evening

Group Type: EXPERIMENTAL

Oral-B Water Flosser

Intervention Type: DEVICE

A water flosser and specialized tip that delivers water with microbubbles of air

Manual toothbrush and dental floss

Brush with a standard ADA manual toothbrush twice daily followed by dental flossing once in the evening

Group Type: ACTIVE_COMPARATOR

Waxed Dental Floss

Intervention Type: DEVICE

Nylon string used to clean between the teeth manually

Interventions

Waterpik Water Flosser

A pulsating water flosser and jet tip designed to clean between the teeth and below the gingival margin.

Intervention Type: DEVICE

Oral-B Water Flosser

A water flosser and specialized tip that delivers water with microbubbles of air

Intervention Type: DEVICE

Waxed Dental Floss

Nylon string used to clean between the teeth manually

Intervention Type: DEVICE

Other Intervention Names

dental water jet; oral irrigator; dental water jet; oral irrigator

Eligibility Criteria

Inclusion Criteria

• Have provided written informed consent prior to being entered into the study.
• Be between 18 and 75 years of age, male or female.
• Have at least twenty (20) natural teeth (5 evaluable in each quadrant) with scorable facial and lingual surfaces as determined by the clinical examiner.
• Nonsmoking (assessed as < 1 cigarette every day for at least a year).
• Have a mean baseline plaque index score of ≥0.60 as determined by the Rustogi Modification of the Navy Plaque Index (RMNPI).
• Have a mean baseline gingival index score of ≥1.75 as determined by the Modified Gingival Index (MGI).
• Have a mean bleeding on probing score of 50%.
• Have probe readings ≤4 mm.
• Agree not to have a dental prophylaxis or any other elective, non-emergency dental procedures any time during the study.
• Agree to abstain from the use of chewing gum, mouth rinses, any toothpaste other than the study toothpaste, tooth whitening products (either professional or at home use) and all other oral hygiene other than the study procedures for the duration of the study.
• Agree to refrain from all oral hygiene on the morning of each evaluation visit and to refrain from eating, drinking or chewing gum for 4 hours prior to each evaluation visit.
• Agree to comply with the conditions and schedule of the study.

Exclusion Criteria

• Physical limitations or restrictions that might preclude normal use of devices.
• Evidence of gross oral pathology, including widespread caries or chronic neglect, extensive restoration, pre-existing gross plaque or soft or hard tissue tumor of the oral cavity.
• Supra- or subgingival calculus that might interfere with evaluations as determined by the clinical examiner.
• Evidence of major oral hard or soft tissue lesions or trauma at the baseline visit as determined by the clinical examiner.
• Conditions requiring antibiotic treatment prior to dental procedures.
• History of uncontrolled diabetes or hepatic or renal disease, or other serious conditions or transmittable disease, (e.g. COVID-19, AIDS).
• Subjects with grossly carious, fully crowned, or extensively restored teeth, orthodontic appliances, peri/oral piercings, or removable partial dentures.
• Treatment with antibiotics within the 1-month period before the baseline examination, or a condition that is likely to require antibiotic treatment over the course of the trial.
• Chronic treatment (2-weeks or more) with any medication known to affect periodontal status (including phenytoin, calcium antagonists, cyclosporine, Coumadin, nonsteroidal anti-inflammatory drugs, and aspirin (325 mg)) within 1- month of the baseline examination. All other medications for chronic medical conditions must have been initiated at least 3 months before enrollment.
• Have moderate to severe periodontal disease or being actively treated for periodontal disease.
• Concomitant periodontal therapy other than prophylaxis in the last 6 months.
• Professional prophylaxis within 1 month prior to the baseline clinical evaluation.
• Subjects who participate in a gingivitis study in the past month.
• History of significant adverse event following use of oral hygiene products such as toothpastes and mouth rinses.
• Subjects who are allergic to any ingredients in Crest® Cavity Protection or Colgate® Cavity Protection toothpaste.
• Self-reported pregnancy or lactating women since hormonal changes can exaggerate gingival response to dental plaque.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Water Pik, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Deborah Mancinelli Lyle

Role: PRINCIPAL_INVESTIGATOR

Water Pik, Inc.

Locations

All Sum Research Center Ltd.

Mississauga, Ontario, Canada

Countries

Canada

Other Identifiers

2021-WP-1

Identifier Type: -

Identifier Source: org_study_id