Trials / Completed
CompletedNCT02186808
T-116_Procera-Bridge Zirconia - A Clinical Study
Procera-Bridge Zirconia - A Clinical Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 80 (actual)
- Sponsor
- Nobel Biocare · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The objective of the study is to evaluate the clinical performance of Procera® Bridge Zirconia veneered with NobelRondo Zirconia.
Detailed description
The study was designed to be an open, 5-year, prospective, multi-center clinical post-market study. The objectives of this clinical study were that industrial centrally produced 3- or 4-unit bridges of yttrium-oxide partially-stabilized (Y-TZP) zirconia (Procera Zirconia) in combination with the veneering ceramic material NobelRondo will show sufficient CDA ratings (90% R+S) and a sufficient survival rate after 1 and 5 years.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Procera® Bridge Zirconia | Patients planned for treatment with a tooth-supported 3 to 4-unit bridge in any position of the maxilla or the mandible. |
Timeline
- Start date
- 2005-05-01
- Primary completion
- 2015-04-01
- Completion
- 2015-04-01
- First posted
- 2014-07-10
- Last updated
- 2016-10-27
- Results posted
- 2016-04-25
Source: ClinicalTrials.gov record NCT02186808. Inclusion in this directory is not an endorsement.