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Comparison of the Effectiveness of Two Different Surgical Therapeutic Protocols of Peri-implantitis

RecruitingNAAges 18 Years - 80 YearsAllNational and Kapodistrian University of Athens
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
Inclusion Criteria: General Inclusion Criteria: * 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 Inclusion Criteria for implants diagnosed with Peri-Implantitis: * 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 * Absence of implant mobility * in participants with more than one implant, the implant with the worst clinical condition will be studied. Inclusion Criteria for implants diagnosed with Peri-Implant Health: * Absence of peri-implant signs of inflammation (redness, swelling) * Lack of bleeding on probing * Absence of bone loss beyond crestal bone level changes resulting from initial remodeling, which should not be ≥2 mm Exclusion Criteria: * Smokers * Uncontrolled diabetes mellitus (HBA1c \>7) * Treatment with bisphosphonates * Needing antibiotic prophylaxis * Currently pregnant or breast-feeding women * History of systemic administration of antibiotic treatment during the preceding 3 months * Systemic conditions that contraindicate treatment * Use of medications known to induce gingival hyperplasia
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What it tests

  • Non-surgical peri-implant therapy
  • Implantoplasty
  • Erythritol Air-abrasive device
  • Prophylaxis
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Where

1 site
Department of Periodontology, School of Dentistry, National and Kapodistrian University of Athens
Athens, Greece
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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