Periodontitis
Conditions
Interventions
A total of 22 participants will be required, from whom three periodontal sites will be selected, and each site will be assigned to one of the three treatment groups: RACR (control), RACR + LBPI (test
E02.594.540
E06.721.189.350
Sponsors
Universidade Federal do Rio Grande do Norte
Universidade Federal do Rio Grande do Norte
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Individuals aged 18 years or older. Both genders. With periodontitis at any stage or degree. Must have suffered attachment loss at two or more non-adjacent interproximal sites. Must have at least three periodontal sites in different quadrants with probing depth - PD equal to or greater than 4 mm, clinical attachment loss (CAL) of 1 mm or more. Bleeding on probing - BOP
Exclusion criteria
Exclusion criteria: Pregnant or lactating individuals. Smokers and individuals who quit smoking within the last five years. Diabetic patients. Individuals who underwent periodontal treatment in the six months prior to the study. Individuals who received antibiotic therapy in the three months prior to the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find better results of probing depth, clinical attachment level, bleeding on probing and radiographic bone density in the test group 1 compared to the test group 2. Clinical parameters will be evaluated through appropriate clinical record, using a North Carolina periodontal probe, at baseline, at 3 and 6 months. Bone densiometric measurement will be performed through periapical radiographs using ImageJ software.;It is expected to find significant reductions in probing depth (PD), clinical attachment level (CAL) and bleeding on probing (BOP), in addition to better radiographic bone density, in the test groups compared to the control group. Clinical parameters will be evaluated through appropriate clinical records, using a North Carolina periodontal probe, at baseline, at 3 and 6 months. Bone densiometric measurement will be performed through periapical radiographs using ImageJ software. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected. | — |
Countries
Brazil
Contacts
Public ContactAna Rafaela Martins
Universidade Federal do Rio Grande do Norte
Outcome results
None listed