Actively Recruiting

Phase Not Applicable
Age: 20Years - 80Years
All Genders
ID05707780

Clinical Evaluation of Resin Matrix Ceramic and Zirconia Posterior Crowns

Led by Universidad Complutense de Madrid · Updated on 2023-02-01

90

Participants Needed

1

Research Sites

173 weeks

Total Duration

On this page

Sponsors

U

Universidad Complutense de Madrid

Lead Sponsor

B

BEGO GmbH

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are conducting a randomized clinical study to compare the survival and success rates, potential biological and technical complications, and overall clinical performance of three types of posterior crowns: metal-ceramic, monolithic zirconia, and resin-matrix ceramic. The study aims to determine if there are any differences among these restorations when used in the back teeth, with a null hypothesis that no differences will be found. This investigation is led by Universidad Complutense de Madrid and focuses on dental materials used for crown restorations. The study will include 60 patients needing a single crown on a molar or premolar in either the upper or lower jaw. Ninety crowns will be made and randomly assigned to one of the three types: resin-matrix ceramic, monolithic zirconia, or metal-ceramic. Treatments will be done by three experienced prosthodontists using standardized tooth preparation methods and full-arch digital impressions taken with an intraoral scanner. Crowns will be cemented with resin cement and all procedures will follow a complete digital workflow. Participants will be monitored at baseline (one week after treatment) and then at 1, 2, and 3 years. Evaluations will include the quality of the restorations, plaque and gingival indices, probing depth, margin stability, and patient satisfaction. Two independent researchers will perform these assessments. The primary outcome is the survival and success rates of the crowns after three years. This study will provide detailed long-term data on the clinical performance of these different crown materials.

CONDITIONS

Brief Title

Clinical Evaluation of Resin Matrix Ceramic Posterior Crowns

Who Can Participate

Age: 20Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • One posterior tooth (molar or premolar) to be crowned
  • Vital abutments or abutments with sufficient endodontic treatment
  • Abutment not crowned previously
  • Periodontally healthy abutments with no signs of bone resorption or periapical disease
  • Adequate occlusogingival height
  • Stable occlusion, and the presence of natural dentition in the antagonist arch
Not Eligible

You will not qualify if you...

  • Patients who present reduced crown length (less than 3 mm occlusogingival height)
  • Poor oral hygiene, high caries activity, active periodontal disease or bruxism

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Single treatment session with follow-up assessments over 3 years

Participants receive one of three types of posterior crowns (resin-matrix ceramic, monolithic zirconia, or metal-ceramic) placed on a posterior tooth following standard preparation and digital impression procedures.

1 baseline visit at 1 week after treatment and follow-up visits at 1, 2, and 3 years

Follow-up

Duration - Up to 3 years after treatment

Participants are monitored to assess the survival, clinical performance, and quality of the crowns, including oral health indices and patient satisfaction.

Follow-up visits at 1, 2, and 3 years

Trial Site Locations

Total: 1 location

1

Faculty of Odontology

Madrid, Spain, 28040

Actively Recruiting

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Research Team

M

MARIA JESUS SUAREZ, PhD

J

JESUS PELAEZ, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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