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Clinical Study on Zirconia Bridges

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01835834
Enrollment
9
Registered
2013-04-19
Start date
2010-01-31
Completion date
2015-12-31
Last updated
2014-07-08

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

Conditions

Missing Teeth

Keywords

zirconia crown

Brief summary

To evaluate the clinical performance and survival rate of NobelProceraTM Bridge Shaded Zirconia on natural teeth in the posterior region for a period of 5 years. The working hypothesis of this clinical study is that industrial centrally produced 3- or 4-unit bridges of shaded yttrium-oxide partially-stabilized (Y-TZP) zirconia (NobelProceraTM Shaded Zirconia) in combination with a veneering ceramic material will show sufficient CDA ratings (80% R+S) and a sufficient survival rate (93%) after 5 years in comparison with a reference level of 95%.

Interventions

PROCEDUREzirconia bridge restoration

Sponsors

University of Siena
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

The subject must be at least 18 (or age of consent), and less than 70 at the time of inclusion. * The subject is healthy and compliant with good oral hygiene * The subject is in need of a posterior fixed partial denture restoration of up to 4 units distal of the canines in the maxilla or mandible. * The subject shall have a stable occlusal relationship with a fully restored, fixed opposing dentition. * Obtained informed consent from the subject the subject should be available for the 5-year term of the investigation. * No apical disorder or inflammation of abutment teeth, adjacent and opposing teeth. * Good gingival / periodontal / periapical status of restoring, opposing and adjacent teeth. Healed situation of soft tissue augmentation is allowed. * The subject should be available for the 5-year term of the investigation.

Exclusion criteria

* The subject is not able to give her/his informed consent to participate. * Alcohol or drug abuse as noted in patient records or in patient history. * Reason to believe that the treatment might have a negative effect on the patient's total situation (psychiatric problems), as noted in patient records or in patient history. * An existing condition where acceptable retention of the restoration is impossible to attain * Mobility of the tooth to be restored. * Pathologic pocket formation of 4 mm or greater around the tooth to be restored * Severe bruxism or other destructive habits * Amount of attached soft tissue is insufficient (no attached gingiva on the buccal side of the tooth). * Health conditions, which do not permit the restorative procedure

Design outcomes

Primary

MeasureTime frameDescription
survival rate of NobelProcera™ Bridge Shaded Zirconia5 yearsSuccess and Failure Criteria The CDA index will be used for the success criteria in this investigation. Please see also the criteria in the clinical parameter part of this protocol. The success and failure criteria to be used in this investigation have been determined as follows: A successful NobelProcera™ Bridge Shaded Zirconia is when: the CDA index is Romeo or Sierra at delivery and remains so during the study period. A surviving NobelProcera™ Bridge Shaded Zirconia is when: the restoration is in occlusion and in function, even though all the success criteria are not fulfilled, but is to be regarded as correctable. A failed NobelProcera™ Bridge Shaded Zirconia is when: the restoration has 1) been removed, 2) fractured, or 3) cannot be classified as a surviving or a successful restoration.

Outcome results

None listed

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