Effects of Biocidin on Oral Biofilms
ConditionBiofilm
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age25+
SponsorOvationLab
About this trial
The primary purpose of this study is to evaluate the effects of Biocidin liquid on oral biofilms among healthy adults. A single-arm, open-label prospective study will be conducted evaluating the impact of two weeks of supplementation with label dosing of Biocidin liquid on oral biofilms as assessed by SimplyPERIO (Spectrum Solutions, Salt Lake City, UT).
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Adult females or males age ≥ 25 years
Ability to read and speak English
Willingness to take use oral Biocidin as directed for two weeks
Willingness not to change any other oral health practices for two weeks
Disqualifiers
Current use of oral Biocidin or botanical mouthwash
Use of antibiotics within the past 30 days
Current use of fixed intraoral orthodontic appliances (e.g., dental braces, fixed retainers, or similar devices)
Known allergies to any of the ingredients in the product
Trial design
Design model
Single group
Treatments tested in this trial
Biocidin Liquid
Dietary supplementBroad-spectrum botanical liquid formula
Treatment groups
60 Participants
are divided into 1 treatment groupGroup A: Biocidin LiquidExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Oral Biofilm Microorganisms
SimplyPERIO - Oral biofilm microorganism test results are categorized as "low", "medium", and "high".
Time frame
Measured at baseline and conclusion of 2-week study Source ClinicalTrials.gov