Clinical Trial

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

Active, Not Recruiting
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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.
Protocol Amendment History 7 amendments
This ClinicalTrials.gov record has been amended 7 times since 2024-01-26; most recent amendment 2025-09-26.
Status change: Recruiting → Active, Not Recruiting 2024-05-24
Status change: Not Yet Recruiting → Recruiting 2024-03-28
Trial Details
NCT Number NCT06238999
Lead Sponsor Ivoclar Vivadent AG
Conditions Non-carious Cervical Lesions
Enrollment 66 participants
Start Date 2024-02-20
Primary Completion 2024-04-30 (estimated)
Study Completion 2029-12-31 (estimated)
Updated on ClinicalTrials.gov 2025-10-23