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Split-mouth Study of a New Flowable Composite in Non-carious Cervical Lesions
Sponsor: Ivoclar Vivadent AG
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.
Official title: Clinical Evaluation of a New Flowable Composite for Direct Restorative Treatment of Non-carious Cervical Lesions: A Prospective Randomized Split-mouth Study
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
66
Start Date
2024-02-20
Completion Date
2029-12-31
Last Updated
2025-10-23
Healthy Volunteers
No
Conditions
Interventions
Restoration of non-carious cervical lesions
Non-carious cervical lesions will be treated with the experimental TM Flow or the well-established Tetric EvoFlow. The treatment workflow is very similar to other flowable composites.
Locations (1)
Ivoclar Vivadent AG
Schaan, Liechtenstein, Liechtenstein