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ACTIVE NOT RECRUITING
NCT07263698
PHASE3

Investigation of Clinical Efficacy of a New Mouthwash on Reducing Dental Plaque and Helping Prevent Gum Problems as Compared to a Control Mouthwash

Sponsor: Colgate Palmolive

View on ClinicalTrials.gov

Summary

Qualified subjects will be enrolled and randomized to either one of the two study groups described above based on their initial modified gingivitis and plaque scores. Subjects will be instructed to use the products according to the instructions provided. Subjects will return to the dental office for evaluation after two weeks, six weeks and three months of product use. All subjects will be followed for adverse events throughout the study

Official title: Investigation of Clinical Efficacy of a New Mouthwash on Reducing Dental Plaque and Helping Prevent Gum Problems as Compared to a Control Mouthwash - a Three-month Study in Italy

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2025-12-01

Completion Date

2026-03

Last Updated

2026-01-14

Healthy Volunteers

Yes

Interventions

DRUG

cetylpyridinium chloride (CPC), zinc lactate and sodium fluoride Mouthwash

0.09% CPC, 0.28% zinc lactate and 500 ppm F as sodium fluoride

DRUG

sodium fluoride Mouthwash

100 ppm F as sodium fluoride

Locations (1)

Clinica Odontoiatrica Montesani

Roma, Rome, Italy