Actively Recruiting
Efficacy of a Stannous Fluoride Toothpaste, Cetylpyridinium Chloride Mouthwash, and Battery Toothbrush Regimen in Reducing Established Dental Plaque and Gingivitis.
Led by Colgate Palmolive · Updated on 2026-02-10
135
Participants Needed
1
Research Sites
12 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To evaluate the efficacy of a stannous fluoride toothpaste, Cetylpyridinium Chloride Mouthwash, and Battery Toothbrush Regimen in Reducing Established Dental Plaque and Gingivitis.
CONDITIONS
Official Title
Efficacy of a Stannous Fluoride Toothpaste, Cetylpyridinium Chloride Mouthwash, and Battery Toothbrush Regimen in Reducing Established Dental Plaque and Gingivitis.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed informed consent form
- Male or female aged 18 to 70 years
- Available for the full 12-week study period
- Generally good health as judged by the investigator
- At least 20 permanent natural teeth, excluding third molars
- Initial gingivitis index of 1.0 or higher by Loe and Silness Gingival Index
- Initial mean plaque index of at least 0.6 by Rustogi Modification of the Navy plaque index
You will not qualify if you...
- Having orthodontic appliances
- Wearing partial removable dentures
- Oral diseases, tumors, or chronic conditions of oral tissues
- Advanced periodontal disease with symptoms like pus, tooth mobility, or extensive bone loss
- Five or more cavities needing immediate treatment
- Use of anticonvulsants, sedatives, tranquilizers, anti-inflammatory or daily pain medications within one month before the study or planned use during the study
- Use of antibiotics within one month before study entry
- Ongoing use of medications affecting gums or other prescription drugs interfering with study outcomes
- Participation in another clinical study
- Pregnancy or breastfeeding
- Dental cleaning within three weeks before baseline exams
- Allergies or history of reactions to oral or personal care products
- Medical conditions preventing eating or drinking for up to 4 hours
- Current smokers or history of alcohol or drug abuse
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Consumer Research Consulting, LLC
Melbourne, Florida, United States, 32935
Actively Recruiting
Research Team
D
Dr. John Gallob, DMD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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