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Clinical Evaluation of a New Dual-cure Universal Adhesive

NCT06615544 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2025-10-23

Study results available
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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

DEVICE

Placement of indirect dental restoration

The newly developed dual-cure adhesive will be used for the placement of indirect restorations.

Sponsors & Collaborators

  • Ivoclar Vivadent AG

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-11-04
Primary Completion
2025-03-27
Completion
2031-04-30

Countries

  • Liechtenstein

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06615544 on ClinicalTrials.gov