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Clinical Trials/NCT05114122
NCT05114122
Unknown
Not Applicable

Clinical Outcomes of Premolars Restored With Ceramic Vonlay Restorations Versus Onlay Using Modified USPHS Criteria (Randomized Clinical Trial)

Cairo University1 site in 1 country26 target enrollmentJanuary 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Clinical Performance of Ceramic Vonlays
Sponsor
Cairo University
Enrollment
26
Locations
1
Primary Endpoint
Fracture
Last Updated
4 years ago

Overview

Brief Summary

Evaluation the clinical performance of premolars restored with ceramic vonlays versus onlays using modified USPHS criteria after follow-up period of 0,3,6,9,12 months

Detailed Description

two groups of patients with vital premolars indicated for fixed restorations will be selected according to special inclusion criteria (n=13) in each group (total of 26). one group will receive minimally invasive cavity preparations for posterior indirect restorations either vonlay or onlay according to each group the patient will be assessed using Modified USPHS Criteria at 0,3,6,9,12 months regarding fracture, marginal integrity and marginal discoloration

Registry
clinicaltrials.gov
Start Date
January 1, 2021
End Date
January 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mohamed Abdel Aziz Hazzaa

Principal Investigator

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Age range of the patients from 25-44 years old, who could read understand and write to sign the consent by himself /herself
  • Have no active periodontal or pulpal diseases, have teeth with good restorations.(19)
  • Psychologically and physically able to withstand conventional dental procedures
  • Patients with teeth problems indicated for onlay and vonlay (premolars).
  • Decayed teeth.
  • Teeth restored with large filling restorations.
  • Able to return for follow-up examinations and evaluation.

Exclusion Criteria

  • Patient less than 25 or more than 44 years.
  • Patient with active resistant periodontal diseases.
  • Patients with poor oral hygiene, high caries risk and uncooperative patients.
  • Pregnant women.
  • Patients in the growth stage with partially erupted teeth.
  • Psychiatric problems or unrealistic expectations.
  • Lack of opposing dentition in the area of interest. 8- The presence of a removable or fixed orthodontic appliance, signs of bruxism or clenching, the absence of more than one unit in the posterior region

Outcomes

Primary Outcomes

Fracture

Time Frame: change from baseline at 3,6,9,12 months

assessed according to modified USPHS criteria (Alpha, Bravo)

Secondary Outcomes

  • Marginal discoloration(0,3,6,9,12 months)
  • Marginal integrity(0,3,6,9,12 months)

Study Sites (1)

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