Influence of Implant Surface Decontamination on the Reconstructive Outcomes of Peri-implantitis
Peri-Implantitis
About this trial
This is an interventional treatment trial for Peri-Implantitis
Eligibility Criteria
Inclusion: Screw-retained or cement-retained fixed or removable implant-supported prosthesis for a minimum of 36 months. All patients in age of 18 to 80 non-smokers no presence of systemic disease or medication known to alter bone metabolism partial or complete edentulous patients that have no active periodontal disease. Exclusion criteria: pregnancy or lactation history of or current smokers uncontrolled medical conditions, lacking keratinized mucosa (≤2mm) on the lingual or buccal implant sites, advanced(A) peri-implantitis (>50% of the implant length).
Sites / Locations
- Clinica CICOMRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Group electrolytic approach (EA)
Group hydrogen peroxide (HP)
Mechanical detoxification using curettes + NiTi brushes + EA (GalvoSurge) during 2 minutes
Group hydrogen peroxide (HP): Mechanical detoxification using curettes + NiTi brushes + hydrogen peroxide 5% for 2 minutes soaked in a gauze