Effects of Biocidin on Oral Biofilms

OvationLab

Status: Enrolling

Conditions: Biofilm

Treatments: Dietary Supplement: Biocidin Liquid

Study type: Interventional

Funder types: NETWORK

Identifiers

NCT07408245

BIO-003

Details and patient eligibility

About

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).

Enrollment: 60 estimated patients

Sex: All

Ages: 25+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Adult females or males age ≥ 25 years
2. Ability to read and speak English
3. Willingness to take use oral Biocidin as directed for two weeks
4. Willingness not to change any other oral health practices for two weeks
5. Willingness not to change dietary habits for two weeks
6. Willingness to perform a SimplyPERIO oral microbiome test before and after the two-week Biocidin intervention

Exclusion criteria

1. Current use of oral Biocidin or botanical mouthwash
2. Use of antibiotics within the past 30 days
3. Current use of fixed intraoral orthodontic appliances (e.g., dental braces, fixed retainers, or similar devices)
4. Known allergies to any of the ingredients in the product
5. Currently pregnant or lactating women or women planning to become pregnant in the next 12 weeks
6. Participants unable to provide consent

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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60 participants in 1 patient group

Biocidin Liquid

Experimental group

Description:

Broad-spectrum botanical liquid formula

Treatment:

Dietary Supplement: Biocidin Liquid