Survival Clinical Trial
Official title:
Clinical Evaluation of Partial Ceramic Posterior Restorations Cemented Using Immediate Dentin Sealing - a (#) Year Follow up From a Retrospective Study.
Verified date | March 2018 |
Source | University Medical Center Groningen |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
A retrospective clinical study will be performed evaluating a large number of partial ceramic
restorations (IPS e-Max press, Ivoclar, Liechtenstein) placed in general practice. Evaluation
will be based on the well established Hickel criteria (Hickel et al, 2010). Rationale:
IPS-e-max press has been made available to the market since 2006. Although millions of these
restorations have been placed worldwide, clinical data are available of less than 200 single
restorations only, covering observation periods of 2-8 years.(Guess et al, 2009; Etman en
Woolford, 2010; Gehrt et al, 2012; Esquivel-Upshaw et al, 2012).
Objective: Study the survival of lithium disilicate restorations during regular check-ups in
a private dental practice.
Status | Completed |
Enrollment | 170 |
Est. completion date | February 2018 |
Est. primary completion date | February 2018 |
Accepts healthy volunteers | |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - In order to be eligible to participate in this study, a patient must received one or more lithium disilicate restorations between 2006 and today. Exclusion Criteria: - No patients will be excluded from the study. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University Medical Center Groningen |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Survival rate | from 2006 to 2018 | ||
Secondary | Quality of survival | according to Hickel | from 2006 to 2018 |
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