None listed
Conditions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.A person who voluntarily signs a clinical research agreement 2.Patients present with =1 implant diagnosed with peri-implantitis 3.Radiographically confirmed peri-implant bone loss >3 mm and probing depth >6 mm, bleeding and/or suppuration on probing
Exclusion criteria
Exclusion criteria: 1.history of surgical treatment for peri-implantitis 2.untreated periodontitis 3.pregnancy 4.intake of drugs affecting periodontal tissues 5.diabetes mellitus, other uncontrolled systemic diseases 6.smoking > 10 cigarettes per day 7.other uncontrolled systemic disease 8.the need of antibiotic prophylaxis and intake of antibiotics within the previous 1 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Treatment success (Composite outcome: PD =5 mm, absence of BOP & no additional bone loss) | — |
Secondary
| Measure | Time frame |
|---|---|
| Clinical measurements;Changes of hard and soft tissue contours (periapical radiographs);Changes of hard and soft tissue contours (intraoral scan); Microbiological analysis; Biomarkers of inflammation;Surgery time | — |
Countries
Korea, Republic of
Contacts
Yonsei University Health System, Dental Hospital