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Clinical Trials/NCT04403230
NCT04403230
Active, not recruiting
Not Applicable

Periodontal and Prosthetic Outcomes on Teeth Prepared With Biologically Oriented Preparation Technique: Prospective Clinical Study

University of Valencia0 sites52 target enrollmentJanuary 1, 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Soft Tissues
Sponsor
University of Valencia
Enrollment
52
Primary Endpoint
A possible periodontal complications
Status
Active, not recruiting
Last Updated
4 years ago

Overview

Brief Summary

The aim of this study is to evaluate the clinical and biological behavior of full coverage restorations on teeth prepared without finish line in a prospective clinical study.

Detailed Description

The purpose is to evaluate the clinical and biological behavior of full coverage restorations on teeth prepared without finish line. This prospective study included 149 teeth treated using biologically oriented preparation technique (BOPT). The sample (149 teeth) was divided into two groups: Seventy four teeth restored with crowns, and 75 teeth supporting fixed partial dentures (FPD). Restorations were fabricated with zirconium oxide cores and ceramic coverings. Patients attended regular annual check-ups when probe depth, presence of inflammation with bleeding on probing, presence of plaque, gingival thickness, marginal stability, biological or mechanical complications, and the patient's level of satisfaction were registered.

Registry
clinicaltrials.gov
Start Date
January 1, 2013
End Date
January 1, 2030
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • adult patients (aged over 18 years).
  • non-smokers.
  • periodontally healthy or periodontally managed.
  • patients who had undergone restoration with fixed prostheses (one-piece crowns or fixed partial dentures FPDs) in the aesthetic zone (incisors, canines, premolars, first molars), which needed to be replaced due to biological, esthetic or some other type of problem.

Exclusion Criteria

  • patients who were smokers.
  • patients who presented unmanaged parafunctional habits.
  • patients with severe systemic diseases.

Outcomes

Primary Outcomes

A possible periodontal complications

Time Frame: Through study completion, an average of 15 years.

Analyze periodontal outcome on teeth prepared with biologically oriented preparation technique

biological or mechanical prosthetic complications

Time Frame: Through study completion, an average of 15 years.

Analyze prosthetic outcome on teeth prepared with biologically oriented preparation technique

Secondary Outcomes

  • Patient's level of satisfaction with treatment assessed by means of a visual analogue scale (VAS).(Through study completion, an average of 15 years.)

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