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Clinical Trials/NCT04775823
NCT04775823
Unknown
Not Applicable

Evaluation of Hybrid Composite-nanoceramic on Material Characteristic and Clinical Use Over Tooth Wear Patients.

National Taiwan University Hospital1 site in 1 country50 target enrollmentMarch 2, 2021
ConditionsDental Wear

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dental Wear
Sponsor
National Taiwan University Hospital
Enrollment
50
Locations
1
Primary Endpoint
Evaluation the change of hybrid composite-nanoceramic on material characteristic and clinical use over tooth wear patients.
Last Updated
5 years ago

Overview

Brief Summary

Evaluation of hybrid composite-nanoceramic on material characteristic and clinical use over tooth wear patients.

Detailed Description

Composite resin is often used to restore patient's dental defficiency, and also the material to cover and protect weak tooth structure. In tooth wear patients, multiple factors attributing to destruct their teeth. The durability and strength of the resotrative material must be reinforced. Nanoceramic infiltrated in composite resin may enhance its mechanical characteristics. Therefore, hybrid composite-nanoceramic material may be effective for tooth wear patients.

Registry
clinicaltrials.gov
Start Date
March 2, 2021
End Date
December 31, 2023
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Evaluation the change of hybrid composite-nanoceramic on material characteristic and clinical use over tooth wear patients.

Time Frame: 3months, 6months, 12months, 24months, 36months

Participants with worn dentition dentition (attrition, erosion, abrasion, abfraction) were enrolled in the present study. They were restored with hybrid composite-nanoceramic resin(Cerasmart, GC Corporation). During the follow up time, participants were examined with clinical photos, radiographic film, intraoral scans, and asked to fill in questionnaires. The questionnaires included subjective questionnaire with VAS scale and objective questionnaire according to FDI criteria. The restorations were evaluated by two observers at baseline and after 3, 6, 12, 24, 36 months according to the FDI criteria, which were categorized into three groups: esthetic parameters (four criteria), functional parameters (six criteria) and biological parameters (six criteria). Restorations were scored for clinical acceptability. Scores 4 and 5 were recorded as clinically unacceptable, and scores 5 was recorded for clinically failed.

Study Sites (1)

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