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Clinical Evaluation of Resin Matrix Ceramic Posterior Crowns

NCT05707780 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2023-02-01

No results posted yet for this study

Summary

The objectives of the present prospective randomized clinical study are to evaluate and to compare the survival and success rates, possible biological and technical complications, and the clinical performance of metal-ceramic, monolithic zirconia and resin-matrix posterior crowns.

The null hypothesis is that no differences would be found between the parameters studied for each type of restoration.

Conditions

  • Dental Materials

Interventions

PROCEDURE

Resin-matrix

posterior crowns

PROCEDURE

Monolithic zirconia

posterior crowns

PROCEDURE

Metal-ceramic

posterior crowns

Sponsors & Collaborators

  • BEGO GmbH

    collaborator UNKNOWN

  • Universidad Complutense de Madrid

    lead OTHER

Principal Investigators

  • MARIA JESUS SUAREZ, PhD · UNIVERSITY COMPLUTENSE OF MADRID

  • JESUS PELAEZ, PhD · UNIVERSITY COMPLUTENSE OF MADRID

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2023-01-25
Primary Completion
2023-07-31
Completion
2026-10-30

Countries

  • Spain

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 NCT05707780 on ClinicalTrials.gov