Actively Recruiting

Phase Not Applicable
Age: 4Years - 9Years
All Genders
Healthy Volunteers
NCT07250022

Detection of Residual Caries on Class II Cavity Walls in Primary Teeth Following Atraumatic Restorative Treatment (ART)

Led by Çanakkale Onsekiz Mart University · Updated on 2026-01-21

212

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The primary aim of this study is to compare the diagnostic agreement and effectiveness of three different methods-Fluorescence-Aided Caries Excavation (FACE), caries detection dye, and clinical observation-in detecting residual caries remaining on cavity walls of primary teeth following Atraumatic Restorative Treatment (ART). Through this comparison, the study seeks to identify the method that provides more reliable and accurate results, thereby contributing to clinical practice by guiding clinicians and supporting the development of strategies to enhance the long-term success of ART.

CONDITIONS

Official Title

Detection of Residual Caries on Class II Cavity Walls in Primary Teeth Following Atraumatic Restorative Treatment (ART)

Who Can Participate

Age: 4Years - 9Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 4-9 years at enrollment
  • Healthy children who can cooperate with dental examination
  • Multi-surface carious cavities that are asymptomatic (no acute symptoms)
  • Written informed consent from parent/guardian and assent from the child
Not Eligible

You will not qualify if you...

  • Acute dental infection present
  • Any systemic disease or condition
  • Lack of cooperation during the procedure
  • Refusal to participate or informed consent/assent not obtained

AI-Screening

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Trial Site Locations

Total: 1 location

1

Canakkale Onsekiz Mart University

Çanakkale, Kepez, Turkey (Türkiye), 17100

Actively Recruiting

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Research Team

B

Burak Çarıkçıoğlu, Associate Professor

CONTACT

İ

İdil Ay Şimşek, Research Assistant

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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