Gingivitis Clinical Trial
Official title:
A 3-Month Clinical Study to Assess the Effects of a Stannous Fluoride Dentifrice on Plaque and Gingivitis
Verified date | December 2019 |
Source | Procter and Gamble |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The objective of this clinical study is to assess the effects of a 0.454% stannous fluoride dentifrice on gingivitis and plaque after 3 months when compared to a negative control.
Status | Completed |
Enrollment | 84 |
Est. completion date | June 3, 2018 |
Est. primary completion date | June 3, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Be at least 18 years of age; - Provide written informed consent prior to participation and be given a signed copy of the informed consent form; - Be in general good health as determined by the Investigator based on a review of the health history/update for participation in the trial; - Have at least 16 gradable teeth; - Agree to return for scheduled visits and follow the study procedures; - Agree to refrain from use of any non-study oral hygiene products for the duration of the study; - Agree to delay any elective dentistry, including dental prophylaxis, until the completion of the study; Exclusion Criteria: - Having taken antibiotic, anti-inflammatory, or anti-coagulant medications within 4 weeks of the Baseline Visit; - Have any oral conditions that could interfere with study compliance and/or examination procedures, such as widespread caries, soft or hard tissue tumor of the oral cavity, or advanced periodontal disease; - Removable oral appliances; - Fixed facial or lingual orthodontic appliances; - Self-reported pregnancy or lactation; - Any diseases or condition that might interfere with the safe participation in the study; and - Inability to undergo study procedures. |
Country | Name | City | State |
---|---|---|---|
United States | University Health Resources Group | Whittier | California |
Lead Sponsor | Collaborator |
---|---|
Procter and Gamble |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Löe-Silness Gingivitis Evaluation | Löe-Silness Gingivitis Evaluation is a validated assessment of gingival health looking at inflammation and bleeding based on a 4 point range 0 (normal gingiva) to 3 (severe inflammation). | Baseline | |
Primary | Löe-Silness Gingivitis Evaluation | Löe-Silness Gingivitis Evaluation is a validated assessment of gingival health looking at inflammation and bleeding based on a 4 point range 0 (normal gingiva) to 3 (severe inflammation). | 1 Month | |
Primary | Löe-Silness Gingivitis Evaluation | Löe-Silness Gingivitis Evaluation is a validated assessment of gingival health looking at inflammation and bleeding based on a 4 point range 0 (normal gingiva) to 3 (severe inflammation). | 3 Months | |
Secondary | Turesky Modified Quigley-Hein Index | The Turesky Modified Quigley-Hein Index is a validated assessment of dental plaque based on a scale of 0 (no plaque/debris) to 5 (plaque covering two-thirds or more of the side of the crown or tooth). | Baseline | |
Secondary | Turesky Modified Quigley-Hein Index | The Turesky Modified Quigley-Hein Index is a validated assessment of dental plaque based on a scale of 0 (no plaque/debris) to 5 (plaque covering two-thirds or more of the side of the crown or tooth). | 1 Month | |
Secondary | Turesky Modified Quigley-Hein Index | The Turesky Modified Quigley-Hein Index is a validated assessment of dental plaque based on a scale of 0 (no plaque/debris) to 5 (plaque covering two-thirds or more of the side of the crown or tooth). | 3 Months |
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