Periodontitis. Renal Insufficiency Chronic Periodontitis
Conditions
Interventions
This clinical study will include two groups of participants, totaling approximately 50 volunteers, distributed as follows: test group (number = 25), patients with chronic kidney disease undergoing dia
at least 30% of sites with probing depth and clinical attachment level equal to or greater than 4 mm, associated with bleeding on probing. Participants in the control group must meet the same criteria
Sponsors
Universidade Federal do Paraná
Universidade Federal do Paraná
Setor de Ciências da Saúde da Universidade Federal do Paraná
Eligibility
Age
30 Years to 80 Years
Inclusion criteria
Inclusion criteria: Volunteers of both sexes; and with the age range from 30 to 80 years. Have at least 10 teeth in the mouth, excluding teeth indicated for extraction. Be patients with chronic kidney disease (test group). Be patients without chronic kidney disease (control group). Have at least 3 teeth with at least 1 interproximal site, not contiguous, with Probing Depth and Clinical Attachment Level of 5 mm, as well as at least 30% of sites with Probing Depth and Clinical Attachment Level of 4 mm and Bleeding on Probing. Patients in the control group will have the same inclusion criteria, except for the presence of chronic kidney disease, and will be matched according to age (plus or minus 3 years) and gender
Exclusion criteria
Exclusion criteria: Pregnant women. Patients who have undergone periodontal treatment in the last six months. Patients who smoke or have smoked within the last five years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected that there will be a reduction in probing depth of at least 15%, as assessed by periodontal examination after 90 and 182 days compared with baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| It has no secondary outcome | — |
Countries
BR
Contacts
Public ContactGabriela Izumi
Universidade Federal do Paraná
Outcome results
None listed