About this trial
The goal of this observational study is to monitor, within a cohort of patients requiring rehabilitation at two different sites in the premolar area, the primary and secondary stability of implants placed with different surface treatments: vacuum-plasma activation, ozonated oil and non-activated implants.
Eligibility criteria
Qualifiers
Age older than 18 years old;
Indication for an implant-supported rehabilitation in the left and right upper premolar/first molar areas;
The area in which the implants will be placed must have had at least 6 months of healing;
No use of grafts or bone substitutes following tooth extraction;
Disqualifiers
Acute myocardial infarction within the previous six months;
Uncontrolled bleeding disorders;
Uncontrolled diabetes (HBA1c > 7.5%);
Radiotherapy in the head-neck area in the previous 48 months;
Trial design
Treatments tested in this trial
- implant with ozonated oil
- non-activated implant
- implant with plasma activation
Treatment groups
Sponsors and collaborators
International Piezosurgery Academy
Lead sponsor
University of Trieste
Collaborator