Periodontal disease, unspecified
Conditions
Interventions
Longitudinal prospective, controlled, randomized, double blind clinical trial. Patients in this study will be allocated to two groups that will receive non-surgical treatment, 28 patients will receive
Drug
Sponsors
Universidade Federal do Rio Grande do Norte
Universidade Federal do Rio Grande do Norte
Departamento de Odontologia da Universidade Federal do Rio Grande do Norte
Eligibility
Inclusion criteria
Inclusion criteria: Present clinical diagnosis of mucositis peri implant, i.e., present probing depth of up to 5 mm, bleeding to the probing without evidence of radiographic bone loss in addition to the first two threads of implants; Be rehabilitated with unitary prosthesis, protocol or overdenture; Be partially or totally toothless; individuals who have been rehabilitated for at least 1 year. For cases of gingivitis, present clinical diagnosis of gingivitis in intact periodont, i.e., present probing depth less than or equal to 3 mm, 10% or more of sites with bleeding to the probing, absence of loss of insertion and bone loss Radiographic Patients presenting sites with probing depth of up to 3 mm, 10% or more of sites with bleeding to the probing, loss of insertion and possible radiographic bone loss; Patients with a history of treatment of periodontitis, therefore, presenting loss of insertion, sites with periodontal pouch of up to 3 mm, 10% or more of sites with bleeding to the probing and radiographic bone loss.
Exclusion criteria
Exclusion criteria: o present systemic complications, such as cardiovascular diseases, Alzheimer's, lung diseases, cerebral or metabolic syndromes;Have used antibiotics, anti-inflammatories, immunosuppressants or periodontal treatment in the last 6 months prior to the survey;Individuals who are in the gestational or breastfeeding period;Individuals who use orthodontic appliances.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find a decrease in inflammation in the peri-implant region, verified by the periodontal probing method, from the decrease in bleeding on probing. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to reduce probing depth and probing bleeding by the periodontal probing method before and after intervention.;The amount of periodontopathogenic bacteria is expected to be reduced by the real time PCR method. | — |
Countries
Brazil
Contacts
Public ContactGuilherme Freire
Departamento de Odontologia da Universidade Federal do Rio Grande do Norte
Outcome results
None listed