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Tooth Wear:m Tooth Wear : Diagnosis- Treatment Decision

Not Applicable
Conditions
Dental Wear
Interventions
Device: Vita-Enamic®
Device: Clearfil Majesty TM
Registration Number
NCT03540264
Lead Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Brief Summary

Tooth wear is a physiological process occurring from normal functioning of the dentition throughout lifetime.

Detailed Description

The studies in the current literature indicated that both techniques of tooth preparation and the materials used are appropriate for the treatment of this condition, but the tendency is to reduce tooth preparation as reasonably possible. In this clinical trial, the investigators will compare the outcomes of direct resin composite and indirect polymer-infiltrated-ceramic-network.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
52
Inclusion Criteria
  • Patients aged 18 years or older, in good general health, willing to participate in the study and accepting to come to regular controls in the future.
  • Patients representing any type of significant tooth wear (≥ 1 mm depth) with dentine exposure in at least 4 teeth: localized tooth wear anterior or posterior teeth and generalized tooth wear anterio and posterior teeth.
  • Patients having posterior support with at least 4 molars in occlusion, 1 pair per side, excluding third molar.
Exclusion Criteria
  • Patients wearing removable partial prosthesis
  • Patients presenting skeletal Cl III occlusal Relationship
  • Patients with remaining clinical crown of ≤ 3 mm in height and presenting tooth anomaly in shape and number in addition to anterior diastemas.
  • Patients with symptomatic temporomandibular joint disorders.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Polymer-infiltrated-ceramic-networkVita-Enamic®This hybrid material seems to be a promising material that imitates natural tooth properties. The VITA-Enamic® will be used in this study.
Composite resinClearfil Majesty TMRestoration with composite resin has shown good clinical performance and limited occlusal wear. The Clearfil Majesty will be used in the present study.
Primary Outcome Measures
NameTimeMethod
Restorationup to 3 years

by modified USPHS criteria

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Cliniques Universitaires Saint-Luc

🇧🇪

Brussel, Belgium

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