N/A
Completed N=80
T-116_Procera-Bridge Zirconia - A Clinical Study
Source: ClinicalTrials.gov NCT02186808 ↗Enrolled (actual)
80
Serious AEs
3.8%
Results posted
Apr 2016
Primary outcomePrimary: Success Rate of Bridge Procera Bridge Zirconia — 100 percentage of successful implants — p=<0.05
Summary
The objective of the study is to evaluate the clinical performance of Procera® Bridge Zirconia veneered with NobelRondo Zirconia.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Success Rate of Bridge Procera Bridge Zirconia |
95.8 | — |
| SECONDARY Success Rate of Bridge Procera Bridge Zirconia |
95.8 | — |
Eligibility Criteria
Inclusion Criteria
- Patients planned for treatment with a tooth-supported 3 to 4-unit bridge in any position of the maxilla or the mandible
- Indication: same indication as for metal supported bridges
- Obtained informed consent from the patient
Exclusion criteria
- Currently known alcohol, drug or medication abuse, judged by the investigator, which might influence the follow-up program
- Patients where a bridge part connection area of 3 mm of diameter is not possible to obtain (short clinical crowns)
- Mobility of the abutment teeth exceeding grade I
- Patients with pathologic pocket formation at abutment teeth
- Patients with complete dentures in the opposing jaw
- Patients with a removable partial denture in the same jaw
Data sourced from ClinicalTrials.gov (NCT02186808). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.