Dental Implants
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patient aged between 18 and 80 years; both sexes; who have had dental implants in place for at least 12 months; diagnosis of peri-implant mucositis is made based on the presence of signs of peri-implant inflammation (redness, edema and bleeding 30 seconds after probing); absence of additional bone loss after initial healing (higher than 2mm)
Exclusion criteria
Exclusion criteria: Pregnant and lactating women; individuals with systemic diseases (osteoporosis, immunological disorders, hepatitis, diabetes mellitus); patients with active periodontitis and peri-implantitis; use of corticosteroids, non-steroidal anti-inflammatory drugs, immunosuppressive drugs, antibiotics, estrogen and estrogen receptor modulators, alentronate and calcitonin during the 6 months prior to the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected that it will be possible to evaluate the effect of using subgingival blasting with erythritol powder on peri-implant mucositis, through the analysis of peri-implant health | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected that it will be possible to evaluate the effect of the use of subgingival blasting with erythritol powder on peri-implant mucositis, through the analysis of peri-implant health, through evaluations of the local profile of anti- and pro-inflammatory mediators and factors related to bone metabolism - IL-1ß, IL-4, IL-6, IL-10, IL-17, TGF-ß, TNF-a, INF-?, DKK1, OC, OPN, OPG, SOST, RANKL, MMP-1, MMP-2, MMP-9 - present in the peri-implant fluid; of the peri-implant microbiome; and of the patient-centered evaluation | — |
Countries
Brazil
Contacts
Universidade Paulista