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Enrolling By InvitationNCT07519382

Comparing the Clinical Success of Two Different CAD/CAM Full Cuspal Coverage Onlays

Comparing the Clinical Success of Milled and 3-D Printed Composite CAD/CAM Full Cuspal Coverage Onlays

Status
Enrolling By Invitation
Phase
N/A
Study type
Interventional
Enrollment
164 (estimated)
Sponsor
Semmelweis University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a single-center, ten-year, randomized controlled, split-mouth clinical trial. A total of 164 adult patients requiring full-cuspal coverage onlays will be enrolled. Each participant will receive one milled and one 3-D printed restoration, randomly assigned.

Detailed description

Restorations will be evaluated at 1 week, 6 months, and 1-10 years using the revised FDI criteria for indirect restorations. The primary outcome is the survival rate of the onlays.

Conditions

Interventions

TypeNameDescription
DEVICEfull cuspal covarage onlayComposite onlays prepared with CAD/CAM technology

Timeline

Start date
2026-04-10
Primary completion
2036-04-18
Completion
2036-12-10
First posted
2026-04-09
Last updated
2026-04-13

Locations

1 site across 1 country: Hungary

Source: ClinicalTrials.gov record NCT07519382. Inclusion in this directory is not an endorsement.

Comparing the Clinical Success of Two Different CAD/CAM Full Cuspal Coverage Onlays (NCT07519382) · Clinical Trials Directory