preventive or screening interventions biomarkers peri-implant bone resorption osteoclastogenesis
Conditions
Interventions
dental implant application using traditional abutments to the posterior site, marginal bone level,dental implant application using platform switch abutments to the posterior site
Active Comparator Device,Active Comparator Device
Sponsors
Istanbul University
Eligibility
Sex/Gender
All
Age
30 Years to 70 Years
Inclusion criteria
Inclusion criteria: Healty patients in need of at least two implants in the posterior region, sites without acute infection or bone defects, at least 7 mm width of available crestal bone for 3.8 or 4.3 mm implants at least 9 mm height of bone.
Exclusion criteria
Exclusion criteria: Patients with systemic medical conditions, such as diabetes, and/or taking any medication(s) that could influence soft and hard tissue healing mechanisms.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Bone loss 12 months Dental radiography,Biomarker analysis 1 and 12 months ELISA | — |
Secondary
| Measure | Time frame |
|---|---|
| Gender distribution 12 months Data analysis | — |
Countries
Turkey
Contacts
Public ContactNecla Kocak Oztug
Istanbul University
Outcome results
None listed