Periodontitis Clinical Trial
Official title:
A Randomized Trial Evaluating the Efficacy of a Gum Health Formulation on Gingival Inflammation, Oral Malodor and Tooth Whitening
The purpose of this study is to evaluate the safety and efficacy of a newly formulated
foaming gel product on gingivitis and/or moderate periodontitis when used with or without
the GLO Science accelerating device (GLO Device), compared to standard tooth brushing with
antioxidant whitening toothpaste with or without flossing (split mouth design for control
group).
This is a 60-day randomized single blinded parallel group study. After 42 days, all use of
interventional products were discontinued, and the participants returned to the clinical
center at day 60 for final measurements. The primary outcomes assessed in this study were
the differences in gingival index (GI) and bleeding on probing (BOP) from baseline to 42 &
60 days. The secondary outcomes are tooth whitening, oral malodor, pocket depth and plaque
amount.
It is hypothesized that participants using the gingival health product with the GLO Device
will experience greater reductions in GI & BOP measurements than the control group, as well
as participants using the gingival health product on a toothbrush alone.
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