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One Year Clinical Evaluation of Conservative Versus Conventional Ceramic Onlays

One Year Clinical Evaluation of Conservative Versus Conventional Ceramic Onlays

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05250232
Enrollment
22
Registered
2022-02-22
Start date
2022-02-27
Completion date
2023-08-12
Last updated
2022-02-22

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

Conditions

Tooth Decay

Brief summary

the aim of present study is to evaluate clinically the fracture liability , marginal adaptation , and patient satisfaction of conservative versus conventional ceramic Onlays use e-max press to restore defective restored molar with old restoration or caries. with one or more cusp defect

Interventions

OTHERonlays conservative

Partial coverage of cusps with shoulder finish line

OTHERonlays conventional

all coverage of cusps as overlay with shoulder finish line

Sponsors

Cairo University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

Inclusion criteria: All subjects are required to be: 1-From 18-50 years old, be able to read and sign the informed consent document. 2- Have no active periodontal or pulpal diseases, have teeth with good restorations 3- Psychologically and physically able to withstand conventional dental procedures 4- Patients with teeth problems indicated for onlay restoration: 1. Decayed teeth 2. Teeth restored with defected filling restorations 3. Teeth with occlusal defect 5- Able to return for follow-up examinations and evaluation

Exclusion criteria

1. Patient less than 18 or more than 50 years 2. Patient with active resistant periodontal diseases 3. Patients with poor oral hygiene 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 \- \-

Design outcomes

Primary

MeasureTime frameDescription
evaluation of fracture resistanceone yearfracture resistance of restorations postoperatively: assessment of the restoration for fracture resistance , by using Measuring device Modified United States Public Health Service (MUSPHS) parameters were used to compare the restorations at baseline and final examination use explorer Measuring unit .Discrete(scores) 1. alpha no evidence of fracture 2. bravo evidence of fracture

Secondary

MeasureTime frameDescription
evaluation of marginal adaptation1 yearmarginal adaptation of restorations postoperatively assessment by Measuring device Modified USPHS Criteria Measuring unit .Discrete(scores) use explorer 1. alpha no visible evidence of ditching along the margin 2. bravo visible evidence of ditching along the margin not extending to the DE junction 3. charlie mismatch between restoration and tooth structure within the normal range of color, shade ,translucency
evaluation of patient satisfaction to the onlay restoration through questioning the patient about pain during eating , acceptability ,sensitivity1 yearpatient satisfaction of restoration use Questionnaire VAS\* Measuring device Measuring unit Numerical(discrete) ('0' unsatisfied-'10' satisfied)

Contacts

Primary ContactHowaida Elhagrasy, M.D.S
howayda.elhagrasy@dentistry.cu.edu.eg01006890707
Backup ContactEman Hussein

Outcome results

None listed

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