Status:
RECRUITING
Efficacy of Different Agents in Treatment of Initial Caries on Smooth Surfaces in Permanent Teeth in Children
Lead Sponsor:
Plovdiv Medical University
Conditions:
White Spot Lesion of Tooth
Eligibility:
All Genders
9-17 years
Phase:
PHASE3
Brief Summary
White spot lesions (WSL) are characterized by an apparently intact outer surface and a demineralized subsurface, and are considered the first clinical sign of dental caries. Aim of this study is to d...
Detailed Description
White spot lesions (WSL) are characterized by an apparently intact outer surface and a demineralized subsurface, and are considered the first clinical sign of dental caries. These lesions are characte...
Eligibility Criteria
Inclusion
- Participants in the study are children 9 to 17 years old.
- Obtained written informed consent from parents or gave-givers as well as obtained verbal informed consent from the child to participate in the study, in which procedures are explained in age-appropriate manner.
- Children, identified as positive or definitely positive through Frankl behavioral rating scale.
- Presence of at least four initial carious lesions of smooth surface (white spots) in permanent teeth that reach the inside of the enamel but are not cavitated, estimated with ICDAS system values 01 (first visible enamel change) and 02 (localized visible enamel change), Nyvad caries activity criteria (1 -active, noncavited lesion) and DIAGNOdent pen values up to 24.
- Study participants did not conduct remineralizing or topical fluorine therapy of the lesions involved up to six months prior to inclusion in the study.
- Children without a history of allergy to the administered medications
Exclusion
- Patients with general diseases or conditions associated with decreased salivation and intake of medications suppressing salivary current. Children with cognitive and behavioral disorders. The presence of a disease is confirmed by an anamnestic interview with the parent.
- Children with a history of allergy to the administered medications
- Patient with non-carious lesion such as enamel hypoplasia, or any developmental defects.
- Patient received restorations or any remineralizing agent other than the regular toothpaste during the last 6 months.
- Participant in another trial.
Key Trial Info
Start Date :
June 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 1 2025
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT05206539
Start Date
June 1 2024
End Date
April 1 2025
Last Update
May 9 2024
Active Locations (1)
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1
Department of Pediatric Dentistry, Faculty of Dental Medicine, Medical University - Plovdiv
Plovdiv, Bulgaria, 4000