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Clinical Evaluation of Internal Fit of Milled BioHPP Polyetheretherketone (PEEK) - Based Versus Zirconia-Based Single Crowns

Clinical Evaluation of Internal Fit of Milled BioHPP Polyetheretherketone (PEEK) - Based Versus Zirconia-Based Single Crowns

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04052789
Enrollment
16
Registered
2019-08-12
Start date
2019-09-01
Completion date
2020-08-01
Last updated
2019-08-13

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

Conditions

Badly Decayed Teeth andTeeth Restored With Large Filling Restorations and Endodontically Treated Teeth and Malformed Teeth and Malposed Teeth

Brief summary

All ceramic crowns are indicated in case of mild to moderate discoloration, restoration of traumatized or fractured teeth and abnormal tooth anatomy. The success of dental restorations is determined by four main factors: biocompatibility, aesthetic value, resistance to fracture and marginal adaptation. . An inadequate marginal fit may compromise the longevity of the restoration since cement film exposure to the oral environment can lead to its dissolution . . Polyetheretherketone (PEEK) is a polymer that has many potentials uses in dentistry. Polyetheretherketone (PEEK) can be used to support fixed dental prostheses. However, information about physio mechanical characterization is still scarce. Aim of the study: \- The aim of this study is to evaluate the internal fit of milled BioHPP PEEK-based versus zirconia-based single crowns.

Interventions

OTHERBioHPP PEEK copings veneered with composite resin

In the first visit, a Face-to-Face adherence session will be held in which the patient should be informed about the study steps and how to maintain oral hygiene measures. Further sessions will occur at the follow-up visits . Participant patients will be asked about any problems they are having. Patients will be recalled every two months for one year for follow up visits.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Masking description

Double(participant, outcome Assessor) Double blind

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* From 18-50 years old, be able to read and sign the informed consent document. * Patient Have no active periodontal or pulpal diseases, have teeth with good restorations * Patient Psychologically and physically able to withstand conventional dental procedures * Patients with teeth problems indicated for single posterior crowns:

Exclusion criteria

* Patient less than 18 or more than 50 years * Patient with active resistant periodontal diseases * Patients with poor oral hygiene and uncooperative patients * Patients in the growth stage with partially erupted teeth * Patient with Psychiatric problems or unrealistic expectations * Patient with Lack of opposing dentition in the area of interest

Design outcomes

Primary

MeasureTime frameDescription
Internal fit of the crown by measuring the thickness of the replica by steriomicroscopeone yearmeasured by replica technique and steriomicroscope

Secondary

MeasureTime frameDescription
secondary caries if present at the margin of the crown by using probeone yearMeasured by modified Ryge criteria Alpha (A)The restoration is a continuation of existing anatomic form adjacent to the restoration. Bravo (B)There is visual evidence of dark keep discoloration adjacent to the restoration (but notAlpha (A)The restoration is a continuation of existing anatomic form adjacent to the restoration. Bravo (B)There is visual evidence of dark keep discoloration adjacent to the restoration (but not directly associated with cavosurface margins). directly associated with cavosurface margins).

Other

MeasureTime frameDescription
patient satisfactionone yearMeasured by VAS(questionnaire)Numerical (discrete) (0 unsatisfied - 10 satisfied)

Contacts

Primary ContactNahla Adly, M.D.S
Dr.nahla.81@gmail.com01010604355
Backup ContactAmina Zaki, professor
aazaki99@yahoo.co.uk

Outcome results

None listed

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