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Zirconia and Metal-based Single Crown Posterior Restorations.

Zirconia-based and Metal-based Single Crown Posterior Restorations: 5-year Results of a Randomized Controlled Clinical Study.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02758457
Enrollment
72
Registered
2016-05-02
Start date
2008-01-31
Completion date
2015-04-30
Last updated
2016-05-02

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

Conditions

Dental Crowns, Dental Prosthesis, Prosthodontics

Keywords

cad/cam, dental porcelain, zirconia, press on metal

Brief summary

The objective of this study was to compare the 5-year survival and clinical behavior of single posterior ceramic crowns made with pressable ceramic on zirconia or on a metal framework. If failures occurred, the further aim of the study was to delineate the factors contributing to the failure. The null hypothesis stated that the survival of zirconia-based restorations would be no worse that those made with metal-based material.

Interventions

DEVICEdental crowns

Sponsors

University of Bologna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Informed Consent as documented by signature * Male and female patients from 18-70 years of age * Need for a single crown restoration * Presence of antagonist * minimum of 20 teeth * moderate to good oral hygiene with the ability to perform mechanical oral hygiene techniques including tooth brushing * low to moderate caries risk, and no active periodontal disease.

Exclusion criteria

* Women who are pregnant at the date of inclusion * Known or suspected non-compliance, drug or alcohol abuse * Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant * Smoking more than 15 cigarettes a day * Poor oral hygiene (Plaque Index over 30%) * Bruxism * vital teeth * allergic reaction or hypersensitivity to ingredients of the adhesive or restorative material

Design outcomes

Primary

MeasureTime frameDescription
Technical complication rate5 yearsassessed by USPHS-criteria

Secondary

MeasureTime frameDescription
Survival rate1, 3, 5 yearsassessed by bleeding on probing

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 9, 2026