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Clinical Trials/NCT05978440
NCT05978440
Not yet recruiting
Not Applicable

Clinical and Laboratory Evaluation of Cad-cam Restorations Fabricated From Digital Impression Under Rubber Dam Isolation (Randomized Clinical Trial & In-vitro Study)

Alexandria University0 sites54 target enrollmentJuly 25, 2023
ConditionsInlays

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Inlays
Sponsor
Alexandria University
Enrollment
54
Primary Endpoint
Evaluate the clinical performance of CAD-CAM onlay restorations fabricated using rubber dam scanning.
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study will be to evaluate the clinical performance of CAD-CAM onlay restorations fabricated using rubber dam scanning techniques up to 12 months and laboratory investigation of their marginal fit.

Detailed Description

A total of 54 molars will be prepared for CAD-CAM onlay restorations. The preparations will be divided into three groups according to the technique of scanning. Group I: 18 preparations will be scanned without rubber dam using standard technique, group II: 18 preparations will be scanned under rubber dam isolation using cut technique, and group III: 18 preparations will be scanned under rubber dam isolation using lock technique. Final restorations will be milled, checked and cemented, then will be evaluated using the modified FDI criteria at baseline, three months, six months, and one year. Thirty resin dies will be 3D printed after scanning of a first molar tooth prepared for onlay. The dies will be scanned after they fit in a typodont and grouped with the same technique (n=10 per group). The digital scans will be superimposed using a 3D best-fit alignment method and 3D deviation will be calculated for each group itself and to the other groups. The marginal fit of the restorations produced will be checked using two methods: Triple scan and measuring the cement thickness after cementation and sectioning of the samples. All data will be collected, and statistically analyzed using suitable tests.

Registry
clinicaltrials.gov
Start Date
July 25, 2023
End Date
December 30, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Healthy adult patients (18-45 years old).
  • Patients in need of class II (OM or OD) caries in molar teeth with initial, moderate or extensive stage according to the staging of caries lesions in The International Caries Detection and Assessment system (ICDASTM codes 2 to 6) (32,33).
  • Presence of proximal caries in digital x-ray with score 2 to 4 according to the ICDAS/ICCMS™ radiographic scoring system(32,33).
  • Vital teeth with absence of clinical signs and symptoms of periapical pathology.
  • Patient Ability to tolerate Rubber Dam applications.
  • Patients who will agree to attend regular check-ups.

Exclusion Criteria

  • Bad oral hygiene (Grade 3)(34).
  • Non- vital teeth or endodontically treated teeth.
  • Severe Periodontal problems (pockets ≥6mm).
  • Patients with para-functional habits (e.g., Bruxism, attrition, wear facets)

Outcomes

Primary Outcomes

Evaluate the clinical performance of CAD-CAM onlay restorations fabricated using rubber dam scanning.

Time Frame: 12 months

Restorations will be evaluated according to three main domains: (40) 1. Functional (domain F): fracture of material and retention(F1), marginal adaptation(F2), proximal contact point(F3), Form and contour(F4), and Occlusion and wear(F5). 2. Biological (domain B): Caries at restoration margins(B1), dental hard tissue defects at restoration margin(B2), postoperative hypersensitivity/pulp status(B3). 3. Aesthetics (domain A): Surface luster and surface texture(A1), Marginal staining(A2), Color match(A3).

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