Status:
COMPLETED
T-116_Procera-Bridge Zirconia - A Clinical Study
Lead Sponsor:
Nobel Biocare
Conditions:
Partial Edentulism
Eligibility:
All Genders
18+ years
Phase:
NA
Brief 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 o...
Eligibility Criteria
Inclusion
- 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
Exclusion
Key Trial Info
Start Date :
May 1 2005
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2015
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT02186808
Start Date
May 1 2005
End Date
April 1 2015
Last Update
October 27 2016
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