NCT06238999

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

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

• Status: Active Not Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 66 (actual)
• Sponsor: Ivoclar Vivadent AG · Industry
• Sex: All
• Age: 18 Years – 65 Years
• Healthy volunteers: Not accepted

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.

Conditions

• Non-carious Cervical Lesions

Interventions

Type	Name	Description
DEVICE	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.

Timeline

• Start date: 2024-02-20
• Primary completion: 2024-04-30
• Completion: 2029-12-31
• First posted: 2024-02-02
• Last updated: 2025-10-23
• Results posted: 2025-05-31

Locations

1 site across 1 country: Liechtenstein