None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The inclusion criteria for this study were (1) presence of clinical peri-implantitis symptoms (PD = 4 mm in two or more aspects around the implant, bleeding and/or suppuration when probing, = 2 mm of bone loss based on radiographic data) and history of surgical treatment (treatment accompanied with flap elevation; regenerative or resective surgery) and (2) presence of radiographic data before and after surgery and during the follow-up period
Exclusion criteria
Exclusion criteria: The exclusion criteria were (1) underwent only non-surgical treatments; (2) no follow-up data or radiographic data after surgical treatment; and (3) more than two surgical treatments with the same implant.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Implant survival status, survival time, | — |
Secondary
| Measure | Time frame |
|---|---|
| degree of implant bone loss | — |
Countries
Korea, Republic of
Contacts
Seoul National University Bundang Hospital