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Clinical Evaluation of Composite-ceramic Implant-supported Posterior Crowns (Cerasmart)

NCT04995458 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2023-01-25

No results posted yet for this study

Summary

The objectives of the present study are to analyze and to compare the survival rates and possible biological and technical complications arising from the use of composite-ceramic posterior implant-supported crowns with those obtained when using their counterparts prepared using monolithic zirconia restorations. The null hypothesis is that no differences would be found between the parameters studied for each type of restoration.

Conditions

  • Dental Materials

Interventions

PROCEDURE

composite-ceramic

To assess the clinical performance of composite-ceramic crowns

PROCEDURE

Monolithic zirconia

To assess the clinical performance of monolithic z¡irconia crowns

Sponsors & Collaborators

  • GC Europe

    collaborator INDUSTRY

  • Universidad Complutense de Madrid

    lead OTHER

Principal Investigators

  • MARIA J SUAREZ, PhD · Universidad Complutense de Madrid

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2017-06-05
Primary Completion
2019-07-20
Completion
2023-06-20

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 NCT04995458 on ClinicalTrials.gov