CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 43 enrolled
Drug / intervention
Experimental Fluoride Applicationdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06166849
NCT06166849N/ACompleted

Clinical Study of Tooth Enamel Remineralization Using DoReMin Product

Ivoclar Vivadent AG·interventional·Posted Dec 12, 2023·Updated Mar 27, 2026

In Brief

A clinical study evaluating Experimental Fluoride Application for White Spot Lesion. Completed, enrolled 43 participants across 1 site.

Detailed Summary

The study is designed as a split-mouth randomised controlled study. This means within the mouth of one patient one tooth with an initial lesion is treated and coated with the Experimental Remineralization product whereas another comparable tooth with an initial lesion is left untreated. Patients are included upon meeting the inclusion criteria as defined for this clinical trial. In the test group, a remineralization of the incipient carious lesion is expected. The patients are recalled after 1 day (optional), 4 weeks, 4 months and finally after 1 year to evaluate the untreated and treated lesion.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesRomania

Timeline

N/ACompletedFinished
202420252026
First PostedDec 12, 2023
Enrollment StartMar 28, 2023
Primary CompletionMay 31, 2024
Study CompletionMar 11, 2025
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 2.6 years ago

Interventions

Experimental Fluoride Applicationdevice

The two-step system, consisting of Component A and Component B, will be applied once on the white spot lesions