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Clinical Trial Summary

This is a clinical investigation to measure the changes in the oral environment resulting from a 3 month exposure to an arginine containing toothpaste. This study is a double blind, randomized controlled, parallel design. Seventy (70) male and female subjects who meet the inclusion/exclusion criteria will be enrolled in the study. Following oral health evaluations, subjects will be assigned to the treatment schedule and receive their assigned study product.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06365047
Study type Interventional
Source Tufts University
Contact Athena Papas, DMD, PhD
Phone 617-636-3931
Email dentalresearchadministration@tufts.edu
Status Recruiting
Phase Phase 3
Start date July 1, 2024
Completion date June 1, 2027

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