Dental implant rehabilitation in adults requiring implants, comparing two implant site preparation techniques and their effects on marginal bone levels and peri-implant clinical parameters Oral Health
Conditions
Interventions
Participants are adults requiring implant rehabilitation in the maxilla and/or mandible who meet predefined eligibility criteria and provide written informed consent. All participants receive bioactiv
a baseline periapical radiograph is taken at surgery.
Participants enter a structured clinical and radiographic follow-up and supportive periodontal care programme with periodic visits (typically eve
Sponsors
Alpha Bio Tec
Eligibility
Sex/Gender
All
Age
30 Years to 85 Years
Inclusion criteria
Inclusion criteria: 1. Patients requiring implant rehabilitation in the maxillary and/or mandibular bone 2. ASA physical status I–II 3. Age between 30 and 85 years 4. Healthy or treated periodontal conditions (treated periodontitis, PI <25%, BoP <25%) 5. Willingness to sign the informed consent and to participate in the clinical study
Exclusion criteria
Exclusion criteria: 1. Absence of type 1–2 post-extraction sites 2. ASA physical status III–IV 3. Untreated periodontitis 4. Sites with a history of previous implant failure 5. Known allergy to one or more medications used during treatment 6. Pregnancy (confirmed by verbal inquiry)
Countries
Italy
Contacts
Public ContactLuigi Canullo
Outcome results
None listed