Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT07575997

Comparison Between Different Interdental Brushes in Adults With Periodontal Disease.

Led by Pierre Fabre Dermo Cosmetique · Updated on 2026-05-08

88

Participants Needed

1

Research Sites

63 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this exploratory study is to evaluate the efficacy of the tested interdental brush versus comparative interdental brushes in adults with periodontal disease, over a 4-week period.

CONDITIONS

Official Title

Comparison Between Different Interdental Brushes in Adults With Periodontal Disease.

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged between 18 and 80 years
  • Signed written informed consent to participate
  • Diagnosed with active generalized periodontal disease (excluding gingivitis)
  • Have at least 20 natural teeth, with 10 teeth on each side (right and left)
Not Eligible

You will not qualify if you...

  • Unable to understand study information or provide written consent due to language or psychiatric reasons
  • Female of childbearing potential who is pregnant, breastfeeding, or plans to become pregnant during the study
  • Having other oral conditions besides periodontal disease or orthodontic conditions that interfere with the study
  • Using systemic or topical mouth treatments that may affect study assessments or planning to use them during the study
  • Received periodontal therapy such as scaling, root planing, or surgery within 2 months before inclusion
  • Had oral or gum surgery within 2 months before inclusion or plans to have such surgery during the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Cliniques universitaires Saint-Luc

Brussels, Belgium, 1200

Actively Recruiting

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Research Team

A

Adeline BACQUEY

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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