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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


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

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