Phase
Condition
N/ATreatment
Non-surgical peri-implant therapy
Implantoplasty
Prophylaxis
Clinical Study ID
Ages 18-80 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
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 patientswho 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 presenceof bleeding on probing and/or suppuration, probing pocket depth ≥6 mm and ≥3 mm ofdetectable bone loss after initial re-modelling
Absence of implant mobility
in participants with more than one implant, the implant with the worst clinicalcondition 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 initialremodeling, which should not be ≥2 mm
Exclusion
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 3months
Systemic conditions that contraindicate treatment
Use of medications known to induce gingival hyperplasia
Study Design
Connect with a study center
Department of Periodontology, School of Dentistry, National and Kapodistrian University of Athens
Athens, 11527
GreeceActive - Recruiting

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