MedTrace Logo

Clinical Evaluation of Monolithic Zirconia FPDs

NCT04879498 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2023-01-25

No results posted yet for this study

Summary

The objectives of the present study are to compare the survival rates and possible biological and technical complications of metal-ceramic, veneered and monolithic zirconia posterior three-unit fixed partial dentures. The null hypothesis is that no differences would be found between the parameters studied for each type of restoration.

Conditions

  • Dental Materials

Interventions

DRUG

Monolithic zirconia

To assess the clinical performance and survival of posterior monolithic zirconia fixed partial dentures

OTHER

Veneered zirconia

To assess the clinical performance and survival of posterior veneered zirconia fixed partial dentures

OTHER

Metal-ceramic

To assess the clinical performance and survival of posterior metal-ceramic fixed partial dentures

Sponsors & Collaborators

  • Ivoclar Vivadent AG

    collaborator INDUSTRY

  • Universidad Complutense de Madrid

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-01-18
Primary Completion
2019-03-30
Completion
2022-12-12

More Related Trials

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 NCT04879498 on ClinicalTrials.gov