Tooth Discoloration Clinical Trial
Official title:
Safety and Efficacy of the ToothWave (Model H7001) Powered Toothbrush Home Use Device for Extrinsic Stain Reduction (Texas)
Verified date | September 2019 |
Source | Home Skinovations Ltd. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study is a single blind, prospective study aimed to evaluate the safety and efficacy of the Silk'n ToothWave Powered Toothbrush for stains reduction and improvement of teeth shade.
Status | Completed |
Enrollment | 91 |
Est. completion date | January 28, 2020 |
Est. primary completion date | January 28, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria 1. Adult subjects aged 18-70, that are in good health. 2. Subjects should have notable extrinsic dental stains on the 6 maxillary labial front teeth, or on the 6 mandibular front teeth (lingual or labial), with a total extrinsic tooth stain score =14 according to the LSI. 3. Subject must have at least 2 natural anterior teeth, each having a mean Lobene composite score of = 1.5 as assessed by the Investigator. 4. Subject front teeth shade should be 9 or darker (meaning shade score should be between 9 and 29), as assessed by the Vita bleachedguide 3D-Master or the Vita EasyShade device. 5. The subjects should understand the information provided about the investigative nature of the treatment, possible benefits and side effects. Subjects will sign the Informed Consent Form. 6. The subjects should be willing to comply with the study procedure and schedule, including the follow up visits, and will refrain from using any other teeth whitening technologies during this period. 7. The subject did not perform any procedure for teeth whitening (either at home or in clinic) at least 3 years prior to participating in the study. Exclusion Criteria 1. Pacemaker or internal defibrillator, or any other active electrical implant anywhere in the body. 2. Pregnant or nursing by subject report. 3. Any active condition in the oral cavity at the discretion of the investigator. 4. Any surgery in the treated area within 3 months prior to treatment, or before complete healing. 5. Subjects that do not brush regularly. 6. Any condition that might make it unsafe for the subject to participate in the study, at the discretion of the investigator. |
Country | Name | City | State |
---|---|---|---|
United States | University of Texas Health Science Center at San Antonio | San Antonio | Texas |
Lead Sponsor | Collaborator |
---|---|
Home Skinovations Ltd. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Extrinsic Stains | Extrinsic Stains will be evaluated using the validated Lobene Stain Index (LSI)
Stain Intensity score range is between 0 and 3, where: 0 = no stain = light stain = moderate stain = heavy stain The mean stain intensity will be calculated for both the gingival and body regions of the incisor teeth for each subject. Stain Area score rage is between 0 and 3, where: 0 = no stain = stain covering up to one third of region = stain covering up to two thirds of region = stain covering more than two thirds of region The mean stain area will be calculated for both the gingival and body regions of the incisor teeth for each subject. |
6 weeks | |
Secondary | Tooth color assessment | VITA Bleachedguide 3D-Master shade guide, includes 29 shade levels defined by the American Dental Association (ADA). These shade levels represents the brightness of the tooth where 1 is the whitest and 29 is the darkest shade. | 6 weeks |
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