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Efficacy of a Eugenol-based Product to Improve the Quality of Toothbrushing and Relieving Gum Discomfort Areas

NCT06366568 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 86

Last updated 2024-04-16

No results posted yet for this study

Summary

The objective of this study is to evaluate the efficacy of a eugenol-based product in improving the quality of toothbrushing and relieving areas of gingival discomfort. This is a randomized, controlled, parallel, examiner-blind clinical trial.

Conditions

  • Plaque, Dental

Interventions

DRUG

fluoride toothpaste containing 1450 ppm of MFP in a PCC base and eugenol gum product

PARTICIPANTS WILL USE A EUGENOL BASED product PRIOR TO TOOTHBRUSHING

DRUG

fluoride toothpaste containing 1450 ppm of MFP in a PCC base

toothbrushing 2x a day for 2 minutes each time

Sponsors & Collaborators

  • Colgate Palmolive

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-02-19
Primary Completion
2024-03-06
Completion
2024-03-06

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06366568 on ClinicalTrials.gov