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Clinical Outcomes of Premolars Restored With Ceramic Vonlay Restorations Versus Onlay Using Modified USPHS Criteria

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05114122
Acronym
vonlay-onlay
Enrollment
26
Registered
2021-11-09
Start date
2021-01-01
Completion date
2022-01-31
Last updated
2021-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Clinical Performance of Ceramic Vonlays

Keywords

Ceramics, vonlay, onlay, fracture

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

Interventions

PROCEDUREVonlay Ceramic restorations

vonlay is a hybrid of an onlay with an extended buccal veneer surface for use in bicuspid regions where there is mostly enamel to bond to. The vonlay is less invasive, more readily repairable, less technique-sensitive to attain adequate bonding, and will leave sounder tooth structure remaining if further treatment is required in the future

PROCEDUREOnlay Ceramic restorations

Onlays are used to restore large areas of decay and also used to replace old restorations, whether they are defective amalgam fillings, old cast-gold onlays, or fabricated from some other material

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Double blinding

Eligibility

Sex/Gender
ALL
Age
25 Years to 44 Years
Healthy volunteers
Yes

Inclusion criteria

1. Age range of the patients from 25-44 years old, who could read understand and write to sign the consent by himself /herself 2. Have no active periodontal or pulpal diseases, have teeth with good restorations.(19) 3. Psychologically and physically able to withstand conventional dental procedures 4. Patients with teeth problems indicated for onlay and vonlay (premolars). 1. Decayed teeth. 2. Teeth restored with large filling restorations. 5. Able to return for follow-up examinations and evaluation.

Exclusion criteria

1. Patient less than 25 or more than 44 years. 2. Patient with active resistant periodontal diseases. 3. Patients with poor oral hygiene, high caries risk and uncooperative patients. 4. Pregnant women. 5. Patients in the growth stage with partially erupted teeth. 6. Psychiatric problems or unrealistic expectations. 7. 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

Design outcomes

Primary

MeasureTime frameDescription
Fracturechange from baseline at 3,6,9,12 monthsassessed according to modified USPHS criteria (Alpha, Bravo)

Secondary

MeasureTime frameDescription
Marginal integrity0,3,6,9,12 monthsassessed according to modified USPHS criteria (Alpha, Bravo, Charlie and Delta)
Marginal discoloration0,3,6,9,12 monthsassessed according to modified USPHS criteria (Alpha, Bravo and Charlie)

Countries

Egypt

Contacts

Primary ContactMohamed Abdel Aziz Hazzaa, PHD
mohamed.hazzaa@dentistry.cu.edu.eg00201066599505
Backup ContactMohamed Abdel Aziz Hazzaa, PHD
mohazza3@gmail.com00201116545475

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026