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Split-mouth Study of a New Flowable Composite in Non-carious Cervical Lesions

Non-carious Cervical Lesions Clinical Trial

Official title:
Clinical Evaluation of a New Flowable Composite for Direct Restorative Treatment of Non-carious Cervical Lesions: A Prospective Randomized Split-mouth Study

Clinical Trial Summary

The overall objective of this clinical investigation is to evaluate the clinical safety and performance of the new flowable composite TM Flow for treatment of non-carious cervical lesions. Each participant receives two different fillings (test- and control material) in two different teeth. The fillings are assessed according to selected FDI criteria at baseline (7-10 days after filling placement) and after 1, 6, 12, 24, 36 and 60 months.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06238999
Study type Interventional
Source Ivoclar Vivadent AG
Contact
Status Recruiting
Phase N/A
Start date February 20, 2024
Completion date December 31, 2029
View Details
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