Clinical Trial

Effect of Toothpastes on Oral Malodor

Completed
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Summary
This study aimed to evaluate the effects of different toothpaste formulations on oral malodor in young adults, addressing the lack of clinical evidence regarding propolis- and probiotic-containing toothpastes, which have predominantly been investigated in mouthrinse, tablet, or chewing gum formulations. Volunteers aged 18-30 years with baseline organoleptic assessment (OA) and Breath Checker® (BC) scores \>0 were randomized into four toothpaste groups: propolis-containing (Glimo Beta), probiotic-containing (Glimo Pi), phosphate-based (Glimo Gamma), and a standard fluoride toothpaste (Sensodyne). Allocation concealment was ensured using identical coded containers, and outcome assessors were blinded. After exclusions, 52 participants completed the study. Oral malodor was evaluated at baseline (T0) and Day 14 (T1) using OA, BC measurements, and self-perceived oral malodor scores.
Trial Details
NCT Number NCT07329062
Lead Sponsor Çankırı Karatekin University
Conditions Oral Malodor (Halitosis)
Enrollment 52 participants
Start Date 2025-01-30
Primary Completion 2025-06-30 (estimated)
Study Completion 2025-12-25 (estimated)
Updated on ClinicalTrials.gov 2026-01-09