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Clinical Performance of Two Different Resin-Matrix Ceramic Restorations

M

Mansoura University

Status

Completed

Conditions

Dental Restoration Failure

Treatments

Other: inlays

Study type

Interventional

Funder types

Other

Identifiers

NCT07265609
J0022055023CD

Details and patient eligibility

About

This study was designed to evaluate and compare the 2-year clinical performance of two different resin-matrix ceramic inlays

Full description

The design of this prospective randomized controlled clinical trial was a split-mouth, two-arm, double-blinded clinical trial, with an allocation ratio of 1:1. The reporting of the trial followed the Consolidated Standards of Reporting Trials (CONSORT) Statement. Twelve adult patients seeking dental treatments in the Conservative Dentistry Department outpatient clinic, Faculty of Dentistry, Mansoura University, were enrolled in the current study with a total of twenty-four compound inlay cavities. Each patient must sign a consent form before participating in the current study. The study was conducted from August 2023 to August 2025 as a part of the doctoral dissertation. Mansoura University's institution's ethics committee approved the form and protocol before conducting the study. The sample size was calculated using the G*Power statistical program. Based on an effect size of 0.4, a significance level of 5% (p < 0.05), and a statistical power of 80%, a minimum of 10 samples per group was required. To compensate for potential dropouts, the total sample size was increased to 12 patients, yielding a total of 24 restorations.

Enrollment

12 patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. The presence of two molars with compound proximal carious lesions or defective restorations involving two surfaces (occluso-mesial or occluso-distal cavities) corresponding to Black's Class II, with a severity score of 4 or 5 according to the International Caries Detection and Assessment System (ICDAS)
  2. The buccolingual width of lesions should exceed two-thirds of the intercuspal distance.
  3. The teeth were required to be vital and free from any periapical radiolucency.
  4. The teeth were required to be in normal alignment, in contact with sound adjacent teeth, and have antagonist teeth present in normal occlusion.

Exclusion criteria

  1. The presence of uncontrolled systemic disease, pregnancy or breastfeeding.
  2. Patients with extremely poor oral hygiene, active periodontal disease, or those involving in orthodontic treatment or periodontal surgery.
  3. Patients with wear facets and parafunctional habits as clinching and bruxism.
  4. Hypersensitive, endodontically treated, non-vital or cracked teeth.
  5. Teeth with proximal cavities involving more than two surfaces, those that exhibited pulp exposure during caries excavation and required direct pulp capping, or those with missing cusps necessitating cusp capping.
  6. Teeth without proximal contact, missing neighbouring or opposing teeth
  7. Patients with known unavailability to attend recall visits, or with known allergy to any component of the study materials.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

12 participants in 2 patient groups

Resin nano-ceramic
Active Comparator group
Description:
Resin-matrix ceramic CAD/CAM blocks for indirect restorations. Restorations were designed, milled, finished, and cemented on the assigned contralateral site according to the manufacturer's instructions. Each patient received this material on one side of the mouth; side allocation was randomized.
Treatment:
Other: inlays
Polymer-infiltrated ceramics
Active Comparator group
Description:
Resin-matrix ceramic CAD/CAM blocks for indirect restorations. Restorations were designed, milled, finished, and cemented on the assigned contralateral site according to the manufacturer's instructions. Each patient received this material on one side of the mouth; side allocation was randomized.
Treatment:
Other: inlays

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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