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Marginal Integrity and Clinical Evaluation of Polyetheretherketone (PEEK) Versus Lithium Disilicate (E-max) Endocrowns.

Marginal Integrity and Clinical Evaluation of Polyetheretherketone (PEEK) Versus Lithium Disilicate (E-max) Endocrowns.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04023357
Enrollment
22
Registered
2019-07-17
Start date
2019-11-30
Completion date
2020-12-31
Last updated
2019-08-08

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

Conditions

Endodontically Treated Teeth

Brief summary

Patients need Endocrowns for their teeth usually use Emax as an etchable ceramic. Yet they have disadvantages that may influence the outcome of the endocrowns, among which is the high stiffness and rigidity owing to the higher modulus of elasticity (67.2 GPa)( compared to natural dentin (18.6 GPa) which may affect the marginal adaptation.so a less rigid material is needed. PEEKs (polyetheretherketones) are presented as alternative materials to metal and glass ceramics, Their elastic modulus comparable to those of cortical bone and dentin so the polymer could exhibit good stress distribution. Also they have high fracture resistance, and low abrasion to the antagonist enamel. .but the investigators have to know clinically it is performance , so the investigators are going to have Parallel groups in a randomized clinical trial.

Interventions

OTHERPEEK

New polyetheretherketones material

OTHEREmax

standard etchable glass ceramic used for Endocrowns

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 60 Years
Healthy volunteers
No

Inclusion criteria

All subjects are required to be: * From 18-60 years old, and able to read and sign the informed consent document. * Physically and psychologically able to tolerate conventional restorative procedures * Have no active periodontal or pulpal diseases. * Willing to return for follow-up examinations and evaluation

Exclusion criteria

* Patients in the growth stage with partially erupted teeth * Patient with fractured teeth of more than 50% enamel loss * Patients with poor oral hygiene and motivation * Pregnant women * Psychiatric problems or unrealistic expectations * Lack of opposite occluding dentition in the area intended for restoration

Design outcomes

Primary

MeasureTime frameDescription
evaluation of marginal gapthrough study completion, an average of 1 yearMarginal gap of the restorations assessed by Silicon replica technique using digital microscope

Secondary

MeasureTime frameDescription
Clinical evaluation of marginal adaptation1 YearMarginal adaptation of the restorations assessed clinically using dental mirror and probe according to the modified united states public health service criteria (USPHS)
Clinical evaluation of fracture resistance1 YearFracture resistance of the restorations assessed clinically using dental mirror and probe according to the modified united states public health service criteria (USPHS)

Other

MeasureTime frameDescription
Clinical evaluation of Retention1 YearRetention of the restorations assessed clinically using dental mirror and probe according to the modified united states public health service criteria (USPHS)

Contacts

Primary ContactAhmed Youssef, M.D.S
Ahmedmohamedosman90@gmail.com01064019439
Backup ContactOmaima Elmahlawy

Outcome results

None listed

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