About this trial
The purpose of the present study is to compare the 1-year clinical, radiographic and microbiological outcomes and patients' satisfaction following surgical treatment of peri-implantitis after applying two different surface modification methods. Secondarily, analysis and comparison of the microbiological results of implants diagnosed and treated for peri-implantitis with healthy implants will be performed.
Eligibility criteria
Qualifiers
Participants ≥ 18 years and ≤ 80 years of age
Non-smokers based on the patients' self-reported smoking status, defined as patients who had never smoked or had quit smoking at least 2 years ago
Implants in function for more than 1 year after suprastructure connection
Presence of at least one implant diagnosed with peri-implantitis defined as presence of bleeding on probing and/or suppuration, probing pocket depth ≥6 mm and ≥3 mm of detectable bone loss after initial re-modelling
Disqualifiers
Smokers
Uncontrolled diabetes mellitus (HBA1c >7)
Treatment with bisphosphonates
Needing antibiotic prophylaxis
Trial design
Treatments tested in this trial
- Non-surgical peri-implant therapy
- Implantoplasty
- Erythritol Air-abrasive device
- Prophylaxis