Determination of the Safety and Efficacy of a Novel Oral Rinse on Oral Health

NCT ID: NCT04197427

Last Updated: 2019-12-17

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 62 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-03-01
• Study Completion Date: 2020-12-31

Brief Summary

Since over 50% of the US population have gingivitis, mouthrinses serve as a valuable adjunct to brushing and flossing. The primary objective is to determine the effectiveness of the oral rinse in reducing plaque and gingivitis and improve a patient's breath

Detailed Description

This clinical study design is a randomized, double-blind, single-treatment, parallel design with a placebo as the control. Following a screening exam, the duration of the trial will be 1 month. Oral examinations will occur at Visit 1 (baseline), and Visit 2 (4 weeks post screening). Also, at these visits, subjects will be asked keep a diary for the one month and their thoughts about the effect of the mouthrinse on their breath and their mouth feeling of "freshness". They will also be asked about the taste and consistency of the mouth rinse. Plaque accumulation will be measured by the Turesky modification of the Quigley-Hein method of quantifying plaque formulation (PI). Gingival health will be measured using the Modified Gingival Index (MGI)

Conditions

Plaque; Gingivitis

Study Design

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

Study Groups

Experimental Oral Rinse

In this arm the test article,oral rinse, a proprietary formulation of agents including xylitol, Caffeine, Essential oils, Monk fruit extract, which can reduce the plaque formation Subjects rinse twice a day with 10 mL of the oral rinse for 2 minutes for 30 days.

They will note, in the daily oral hygiene diary, the date and time of brushing and rinsing.

Group Type: EXPERIMENTAL

Experimental Oral Rinse

Intervention Type: DEVICE

Experimental Oral Rinse is a proprietary formulation of GRAS ingredients

Placebo Oral Rinse

This arm will use a placebo with out the active ingredients same way the experimental arm do.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DEVICE

Placebo formulation without the active ingredients

Interventions

Experimental Oral Rinse

Experimental Oral Rinse is a proprietary formulation of GRAS ingredients

Intervention Type: DEVICE

Placebo

Placebo formulation without the active ingredients

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Subject has read, signed and received a copy of the Informed Consent and HIPAA authorization prior to study initiation.
• Subject is able to follow verbal and/or written instructions, perform oral hygiene procedures and return to the test facility for specified study examinations.
• Subject is between the ages of 18 and 75 years inclusive.
• Subject will not have professional cleaning during the study.
• Subject has no history of allergy to personal care consumer products, or their ingredients, relevant to any ingredient in the test drug, as determined by the Principal Investigator.
• Subject has a minimum of 12 natural teeth.
• Subject agrees to refrain from the use of any oral rinse, toothpaste or dentifrice other than the Aim® Fluoride toothpaste and study rinse provided on Visit 1 for the duration of the study.
• Subject agrees to refrain from the use of other oral care products not supplied by the study center
• Subject agrees to be compliant with study procedures.
• Females of childbearing potential agree to use an adequate method of birth control and agree to pregnancy

Exclusion Criteria

• Subject has read, signed and received a copy of the Informed Consent and HIPAA authorization prior to study initiation.
• Subject is able to follow verbal and/or written instructions, perform oral hygiene procedures and return to the test facility for specified study examinations.
• Subject is between the ages of 18 and 75 years inclusive.
• Subject will not have professional cleaning during the study.
• Subject has no history of allergy to personal care consumer products, or their ingredients, relevant to any ingredient in the test drug, as determined by the Principal Investigator.
• Subject has a minimum of 12 natural teeth.
• Subject agrees to refrain from the use of any oral rinse, toothpaste or dentifrice other than the Aim® Fluoride toothpaste and study rinse provided on Visit 1 for the duration of the study.
• Subject agrees to refrain from the use of other oral care products not supplied by the study center
• Subject agrees to be compliant with study procedures.
• Females of childbearing potential agree to use an adequate method of birth control and agree to pregnancy testing at the first and second visit.

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

Sponsors

You First Services

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Department of Periodontics and Endodontics,School of Dental Medicine, University at Buffalo, SUNY

Buffalo, New York, United States

Countries

United States

Central Contacts

Sebastian Ciancio, D.D.S

Role: CONTACT

Phone: 716-829-3848

Email: ciancio@buffalo.ed

Other Identifiers

SW-101-19

Identifier Type: -

Identifier Source: org_study_id