The Clinical of Stannous Fluoride Toothpaste and a Newly Designed Toothbrush Compared to Colgate Cavity Protection Toothpaste and a Regular Toothbrush in Reducing Plaque and Gingivitis.
NCT06427499 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 95
Last updated 2026-03-19
Summary
Qualified subjects will be enrolled and randomly assigned to either of the two study groups based on their initial Plaque and Gingivitis scores. During the first visit, subjects will undergo three key procedures: 1) evaluation for baseline plaque and gingivitis, 2) brushing with the assigned regimen products for two minutes, and 3) assessment for post-brushing plaque only. Subjects will be provided with clear instructions for regimen product usage and will be expected to adhere to these instructions. Follow-up evaluations for plaque and gingivitis will be conducted at one week, six weeks, and three months after initiation of regimen product use. Throughout the study period, continuous monitoring for adverse events will be carried out for all subjects.
Conditions
- Plaque
- Gingivitis
Interventions
- DRUG
-
Stannous fluoride toothpaste
brush 2 min morning \& night daily
- DRUG
-
Colgate Cavity Protection Toothpaste
brush 2 min morning \& night daily
Sponsors & Collaborators
-
Colgate Palmolive
lead INDUSTRY
Principal Investigators
-
Terdphong Triratana · M U International Oral Science Research, Ltd
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2024-04-22
- Primary Completion
- 2024-08-05
- Completion
- 2024-08-05
- FDA Drug
- Yes
Countries
- Thailand
Study Locations
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