NCT06615544

Clinical Evaluation of a New Dual-cure Universal Adhesive

Clinical Evaluation of a New Dual-cure Universal Adhesive for Indirect Restorative Treatment

• Status: Active Not Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 45 (actual)
• Sponsor: Ivoclar Vivadent AG · Industry
• Sex: All
• Age: 18 Years – 65 Years
• Healthy volunteers: Not accepted

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.

Conditions

• Class I Dental Restorations
• Class II Dental Restorations
• Insufficient Dental Restoration
• Caries, Dental

Interventions

Type	Name	Description
DEVICE	Placement of indirect dental restoration	The newly developed dual-cure adhesive will be used for the placement of indirect restorations.

Timeline

• Start date: 2024-11-04
• Primary completion: 2025-03-27
• Completion: 2031-04-01
• First posted: 2024-09-26
• Last updated: 2025-10-23
• Results posted: 2025-08-19

Locations

1 site across 1 country: Liechtenstein