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Wear of Enamel Antagonist to Two Different Types of Monolithic Zirconia Monolithic Zirconia

Wear of Enamel Antagonist to Two Different Types of Monolithic Zirconia: A Randomized Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04798300
Enrollment
26
Registered
2021-03-15
Start date
2021-09-01
Completion date
2022-09-01
Last updated
2021-06-18

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

Conditions

Wear, Occlusal

Brief summary

The aim of the present study is to evaluate the wear of enamel opposed by Newly Introduced Gradient Monolithic Zirconia compared to that of enamel opposed by Full Strength Monolithic Zirconia

Detailed description

The aim of the present study is to evaluate the wear of enamel opposed by Newly Introduced Gradient Monolithic Zirconia compared to that of enamel opposed by Full Strength Monolithic Zirconia Teeth preparation and impressions, placement and permanent cementation of the final restoration using resin cement, and optical scanning of both the restoration and the opposing tooth. Follow up postoperatively after six and twelve months, and optical scanning of both the restoration and the opposing tooth.

Interventions

PROCEDURENewly Introduced Gradient Monolithic Zirconia

Fabrication of full-coverage crowns over posterior teeth using Newly Introduced Gradient Monolithic Zirconia to measure wear

PROCEDUREFull Strength Monolithic Zirconia

Fabrication of full-coverage crowns over posterior teeth using Full Strength Monolithic Zirconia to measure wear

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 50 Years
Healthy volunteers
Yes

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 planned for a single coverage restoration in the posterior area. 5. Patients with a natural (not crowned) opposing antagonist. 6. Able to return for follow-up examinations and evaluation.

Exclusion criteria

* Patient less than 18 or more than 50 years 2. Patients with severe clenching or bruxing habits. 3. Patient with active resistant periodontal diseases 4. Patients with poor oral hygiene and uncooperative patients 5. Pregnant women 6. Patients in the growth stage with partially erupted teeth 7. Psychiatric problems or unrealistic expectations 8. Lack of opposing dentition at the area of interest. 9. Presence of dental prosthesis in the opposing arch at the area of interest.

Design outcomes

Primary

MeasureTime frameDescription
Enamel wear of teeth opposing the restorations to be tested opposing to tested restorationsone yearmeasured by Geomagic professional software

Secondary

MeasureTime frameDescription
Wear of restorations to tested opposed to natural teethone yearmeasured by Geomagic professional software

Outcome results

None listed

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