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Clinical Trials/NCT04879498
NCT04879498
Completed
Not Applicable

Clinical Evaluation of Monolithic Zirconia and Metal-ceramic Posterior Fixed Partial Dentures

Universidad Complutense de Madrid0 sites90 target enrollmentJanuary 18, 2016

Overview

Phase
Not Applicable
Intervention
Monolithic zirconia
Conditions
Dental Materials
Sponsor
Universidad Complutense de Madrid
Enrollment
90
Primary Endpoint
Quality of restorations at baseline
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The objectives of the present study are to compare the survival rates and possible biological and technical complications of metal-ceramic, veneered and monolithic zirconia posterior three-unit fixed partial dentures. The null hypothesis is that no differences would be found between the parameters studied for each type of restoration.

Detailed Description

Ninety patients requiring at least one 3-unit Fixed partial denture (FPD) in the posterior region of the maxilla or mandible were included in this study. All subjects were recruited from the Master in Buccofacial Prostheses and Occlusion (Faculty of Odontology, University Complutense of Madrid, Spain). Before treatment, patients were informed of the study objectives, clinical procedures, materials used, advantages and possible risks of the ceramic material, and other therapeutic alternatives. Prior to the study, participants were asked to provide written informed consent. Ninety posterior FPDs were produced and allocated in parallel and randomly to either monolithic zirconia, veneered zirconia or MC restorations. The clinical procedures were performed by two experienced clinicians. All participants received oral hygiene instructions and a professional tooth cleaning prior to prosthetic treatment. The abutment teeth were prepared with a 0.8- to 1-mm-wide circumferential chamfer, an axial reduction of 1 mm and an occlusal reduction of 1.5- to 2.0-mm. A 10- to 15- degree angle of convergence was achieved for the axial walls. Tooth preparations were scanned with an intraoral scanner and the FPDs were designed using specific software. The restorations were then cemented using a resin self-adhesive cement. After cementation, occlusal contacts were evaluated, and the adjusted surfaces were polished using a porcelain polishing kit. The 90 FPDs were examined at 1week (baseline),1, 2 and 2 years by 2 researchers who were not involved in the restorative treatment.

Registry
clinicaltrials.gov
Start Date
January 18, 2016
End Date
December 12, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • One posterior tooth (molar or premolar) to be replaced
  • Vital abutments or abutments with an adequate endodontic treatment
  • Abutment not crowned previously
  • Periodontally healthy abutments with no signs of bone resorption or periapical disease
  • Adequate occlusogingival height for an appropiate connector area of at least 9 mm2
  • Stable occlusion and the presence of natural dentition in the antagonist arch.

Exclusion Criteria

  • Patients who require a Fixed Dental Prosthesis of more than three units
  • Patients who present reduced crown length (less than 3 mm occlusogingival heigth)
  • Poor oral hygiene, high caries activity, or active periodontal disease

Arms & Interventions

Monolithic zirconia

Monolithic zirconia posterior 3-unit fixed partial dentures

Intervention: Monolithic zirconia

Veneered zirconia

Veneered zirconia posterior 3-unit fixed partial dentures

Intervention: Veneered zirconia

Metal-ceramic

Metal-ceramic posterior 3-unit fixed partial dentures

Intervention: Metal-ceramic

Outcomes

Primary Outcomes

Quality of restorations at baseline

Time Frame: Baseline

The quality of the surface and color, anatomical form and marginal integrity was assessed using the California Dental Association's assessment system. Each CDA criterion was ranked on a scale of 1 to 4, where 4 = excellent, 3 = good, 2 = unacceptable (repair), and 1 = unacceptable (replacement).

Plaque Index (PI) at 2 years

Time Frame: 2 years

Plaque Index (PI) of the abutment and control teeth. A score of 0 to 3 was assigned. Higher score means a worse outcome.

Quality of restorations at 2 years

Time Frame: 2 years

The quality of the surface and color, anatomical form and marginal integrity was assessed using the California Dental Association's assessment system. Each CDA criterion was ranked on a scale of 1 to 4, where 4 = excellent, 3 = good, 2 = unacceptable (repair), and 1 = unacceptable (replacement).ty was assessed

Quality of restorations at 3 years

Time Frame: 3 years

The quality of the surface and color, anatomical form and marginal integrity was assessed using the California Dental Association's assessment system. Each CDA criterion was ranked on a scale of 1 to 4, where 4 = excellent, 3 = good, 2 = unacceptable (repair), and 1 = unacceptable (replacement).

Plaque Index (PI) at 1 year

Time Frame: 1 year

Plaque Index (PI) of the abutment and control teeth. A score of 0 to 3 was assigned. Higher score means a worse outcome.

Plaque Index (PI) at 3 years

Time Frame: 3 years

Plaque Index (PI) of the abutment and control teeth. A score of 0 to 3 was assigned. Higher score means a worse outcome.

Gingival Index (GI) at 1 year

Time Frame: 1 year

Gingival Index (GI) of the abutment and control teeth. A score of 0 to 3 was assigned. Higher score means a worse outcome.

Gingival Index (GI) at 2 years

Time Frame: 2 years

Gingival Index (GI) of the abutment and control teeth. A score of 0 to 3 was assigned. Higher score means a worse outcome.

Margin stability at 2 years

Time Frame: 2 years

To assess the gingival margin stability throughout the evaluation period (subgingival, isogingival or supragingival)

Probing depth at 3 years

Time Frame: 3 years

Probing depth of the abutment and control teeth. A score of 0 to 4 was assigned. Higher score means a worse outcome

Gingival Index (GI) at baseline

Time Frame: Baseline

Gingival Index (GI) of the abutment and control teeth. A score of 0 to 3 was assigned. Higher score means a worse outcome.

Margin stability at 1 year

Time Frame: 1 year

To assess the gingival margin stability throughout the evaluation period (subgingival, isogingival or supragingival)

Margin stability at 3 years

Time Frame: 3 years

To assess the gingival margin stability throughout the evaluation period (subgingival, isogingival or supragingival)

Quality of restorations at 1 year

Time Frame: 1 year

The quality of the surface and color, anatomical form and marginal integrity was assessed using the California Dental Association's assessment system. Each CDA criterion was ranked on a scale of 1 to 4, where 4 = excellent, 3 = good, 2 = unacceptable (repair), and 1 = unacceptable (replacement).

Plaque Index (PI) at baseline

Time Frame: Baseline

Plaque Index (PI) of the abutment and control teeth. A score of 0 to 3 was assigned. Higher score means a worse outcome.

Gingival Index (GI) at 3 years

Time Frame: 3 years

Gingival Index (GI) of the abutment and control teeth. A score of 0 to 3 was assigned. Higher score means a worse outcome.

Probing depth at 1 year

Time Frame: 1 year

Probing depth of the abutment and control teeth. A score of 0 to 4 was assigned. Higher score means a worse outcome

Margin stability at baseline

Time Frame: Baseline

To assess the gingival margin stability throughout the evaluation period (subgingival, isogingival or supragingival)

Probing depth at baseline

Time Frame: Baseline

Probing depth of the abutment and control teeth. A score of 0 to 4 was assigned. Higher score means a worse outcome

Probing depth at 2 years

Time Frame: 2 years

Probing depth of the abutment and control teeth. A score of 0 to 4 was assigned. Higher score means a worse outcome

Patient satisfaction at 3 years

Time Frame: 3 years

Subjective patient satisfaction using Visual analogue scale (VAS) ranged from 0 (worst possible result) to10 (best possible result). The items analyzed were: esthetics, function, comfort, overall satisfaction

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