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Efficacy Evaluation of Two Different Fluoride Applications

NCT06131294 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 23

Last updated 2025-10-23

Study results available
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Summary

The goal of this clinical trial is to evaluate the remineralizing or preservative effect of two different fluoride-containing products. The main question aims to answer how the mineral content of the active white spot lesions change after the treatment with those two fluoride applications in a split-mouth design by measuring their mineral content via QLF technology.

Each patient will receive both treatments in a split-mouth design. It is comparison between an experimental fluoride application and Fluoride Protector S.

Conditions

  • White Spot Lesion

Interventions

DEVICE

Fluoride Application (Experimental Fluoride Application)

Fluoride containing applications are applied on white spot lesions. First solution was air-dried before the second application with the other component was done.

DEVICE

Fluor Protector S

Fluor Protector S is applied on white spot lesions.

Sponsors & Collaborators

  • Istanbul Medipol University Hospital

    collaborator OTHER

  • Ivoclar Vivadent AG

    lead INDUSTRY

Principal Investigators

  • Burcu Gözetici, Dr. · Istanbul Medipo University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
13 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-24
Primary Completion
2023-05-31
Completion
2024-04-16

Countries

  • Turkey (Türkiye)

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 NCT06131294 on ClinicalTrials.gov