Clinical Trial

Clinical Evaluation of a New Dual-cure Universal Adhesive

Active, Not Recruiting
View on ClinicalTrials.gov →
Summary
The overall aim of this study is to evaluate the clinical performance and safety of the new dental dual-cure adhesive for luting indirect ceramic restorations (inlays and onlays). The primary aim is to determine the rate of postoperative hypersensitivity occurrence after using the new adhesive for the placement of indirect restorations. The secondary objective of this study is to assess the long-term clinical performance of the new adhesive in terms of marginal quality, retention/fracture rate of the ceramic restorations, and vitality/fracture rate of the restored teeth.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2024-09-24; most recent amendment 2025-09-26.
Status change: Recruiting → Active, Not Recruiting 2025-08-18
Status change: Not Yet Recruiting → Recruiting 2025-01-10
Trial Details
NCT Number NCT06615544
Lead Sponsor Ivoclar Vivadent AG
Conditions Class I Dental Restorations, Class II Dental Restorations, Insufficient Dental Restoration, Caries, Dental
Enrollment 45 participants
Start Date 2024-11-04
Primary Completion 2025-03-27 (estimated)
Study Completion 2031-04 (estimated)
Updated on ClinicalTrials.gov 2025-10-23