Actively Recruiting
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
Eligibility Criteria
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
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
AI-Powered Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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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