Single Brushing Plaque Removal Efficacy of a Battery-powered Toothbrush and a Manual Toothbrush

NCT ID: NCT06126445

Last Updated: 2024-02-28

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 62 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-11-13
• Study Completion Date: 2024-01-12

Brief Summary

To evaluate and compare the plaque removal efficacy of a battery-powered toothbrush and a manual toothbrush following a single brushing.

Detailed Description

This is a single use, examiner blinded, randomized, two-period, cross-over, IRB-approved research study evaluating the single-use plaque removal efficacy of a new battery-operated toothbrush and a marketed manual toothbrush. This study will accept up to 64 subjects, 18-65 years of age, in anticipation that 60 subjects will complete the study. Qualified subjects with sufficient plaque, according to Rustogi Modified Navy Plaque Index (RMNPI) will be randomly assigned to one of two sequence treatment groups.

After the pre-brushing plaque evaluation at each of the evaluation visits, subjects will brush with the assigned toothbrush and toothpaste provided for timed brushing under supervision, in front of mirror.

Conditions

Plaque, Dental

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Battery operated toothbrush

battery operated toothbrush

Group Type: ACTIVE_COMPARATOR

Battery operated toothbrush

Intervention Type: DEVICE

Device on plaque removal efficacy

Manual toothbrush

Manual toothbrush

Group Type: ACTIVE_COMPARATOR

Manual toothbrush

Intervention Type: DEVICE

Device on plaque removal efficacy

Interventions

Battery operated toothbrush

Device on plaque removal efficacy

Intervention Type: DEVICE

Manual toothbrush

Device on plaque removal efficacy

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Have provided a signed and dated informed consent document indicating that you have been informed of all pertinent aspects of the study before any assessments are performed. You will receive a copy of the signed informed consent.

2. Be between 18 and 65 years of age (inclusive), male or female.

3. Able to brush their own teeth on a daily basis.

4. Be in good health based on medical history review by the Principal Investigator.

5. Have a minimum of at least 18 natural, gradable teeth.

6. Have a mean full-mouth pre-brushing plaque score (Rustogi Modification of the Navy Plaque Index, RMNPI) of ≥ 0.50 at evaluation visits 2 & 3.

7. Have agreed to refrain from use of all oral hygiene products (i.e. floss, mouthwash, etc.), other than the toothbrush and toothpaste supplied, for the duration of the study including the acclimation periods.

8. Have agreed to refrain from all oral hygiene and chewing gum for approximately 12-16 hours and refrain from eating, drinking, smoking and chewing gum for approximately 4 hours prior to Visits 2 & 3.

9. Have agreed 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.

10. Approximately 50% of subjects will be regular electric toothbrush users and 50% of subjects will be regular manual toothbrush users.

11. Have agreed to comply with the conditions and schedule of the study.

Exclusion Criteria

1. Have any physical limitations or restrictions which might preclude normal tooth brushing.

2. Have to be premedicated prior to dental treatment.

3. Have evidence of poor oral hygiene or rampant dental caries or calculus deposits that may interfere with plaque assessments.

4. Have evidence of major oral hard or soft tissue lesions or trauma at Baseline.

5. Have fixed or removable orthodontic appliances.

6. Have received a dental prophylaxis within a month prior to Visit 1.

7. Have a history of a significant adverse event, allergy, or irritation that was due to oral hygiene products.

8. Have participated in another dental research study within 4 weeks prior to Visit 1.

9. Therapy with any medications, currently or within the last 28 days, which might interfere with the outcome of the study by affecting tissue condition, or salivation, particularly chronic therapy or long-term use, as determined by the investigator.

10. Existing serious medical condition or transmittable disease as determined by the Principal Investigator after review of the medical history form. These will include but not be limited to, hepatitis, tuberculosis, AIDS.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Church & Dwight Company, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jimmy Qaqish

Role: STUDY_DIRECTOR

All Sum Research Center Ltd.

Locations

All Sum Research Center Ltd.

Mississauga, Ontario, Canada

Countries

Canada

Other Identifiers

ST-23-U34

Identifier Type: -

Identifier Source: org_study_id