Clinical Evaluation of an Experimental Remineralization Product

Status Active, not recruiting

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

White Spot Lesion

Clinical Trial Details

NCT number	NCT06166849
Study type	Interventional
Source	Ivoclar Vivadent AG
Contact
Status	Active, not recruiting
Phase	N/A
Start date	March 28, 2023
Completion date	April 30, 2025

View Details

See also
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