Conventional and Ultrasonic Implant Site Preparation (PI-DRI)
Bone Atrophy, Alveolar
About this trial
This is an interventional treatment trial for Bone Atrophy, Alveolar focused on measuring implant, piezoelectric, drills, immediate loading
Eligibility Criteria
Inclusion Criteria:
indications for two implant-supported single crowns with immediate loading in the upper or lower arch (in the incisor, canine or premolar area), based on accurate diagnosis and treatment planning; 2) implants can be in the same or in different quadrants; 3) implant sites must be performed in similar bone quality (i.e. both maxillary or mandibular); 4) the bone crest must be healed (at least three months elapsed after tooth loss); 5) presence of a residual bone crest with an adequate volume to allow the insertion of a 3.8x11.5 mm implant without any kind of regenerative procedure; 6) age of the patient >18 years; 7) patient willing and fully capable to comply with the study protocol; 8) written informed consent given;
Exclusion Criteria:
- acute myocardial infarction within the past 2 months;
- uncontrolled coagulation disorders;
- uncontrolled diabetes (HBA1c > 7.5%);
- radiotherapy to the head/neck district within the past 24 months;
- immunocompromised patient (HIV infection or chemotherapy within the past 5 years);
- present or past treatment with intravenous bisphosphonates;
- psychological or psychiatric problems;
- alcohol or drugs abuse Local exclusion criterion is the presence of uncontrolled or untreated periodontal disease (full mouth plaque score and full mouth bleeding score > 25%)
Sites / Locations
- Piezosurgery Academy
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
edentulism side 1
edentulism side 2
ultrasound implant site preparation
conventional implant site preparation