Periodontitis
Conditions
Interventions
This is a double-blind randomized controlled clinical study. Experimental group: 25 patients with periodontal disease but without systemic diseases who will receive surgical periodontal therapy and a
Sponsors
Universidade de São Paulo
Universidade de São Paulo
Eligibility
Inclusion criteria
Inclusion criteria: Patients of both sexes; should have completed periodontal therapy related to the cause more than a month ago and still have sites with 2 or more adjacent teeth presenting pockets with a probing depth greater than or equal to 5 mm; with bleeding on probing and/or suppuration; and also good standards of oral hygiene (plaque index (PI) = 25% and bleeding on probing index (IBP) = 20%)
Exclusion criteria
Exclusion criteria: Patients should not have systemic conditions that could interfere with post-surgical repair, such as diabetes; they should not use medications that affect the gums and/or oral mucosa (phenytoin and other antiepileptic agents; cyclosporine; calcium channel blocking agents); they could not be smokers; pregnant or breastfeeding patients; patients who had a history of allergy to any of the components to be used in the present study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to clinically evaluate patients by checking the probing depth using a millimeter periodontal probe North Carolina | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to count the averages of 40 bacterial species present through analysis of subgingival biofilm samples;It is expected to clinically evaluate patients by checking the clinical level of attachment using a millimeter periodontal probe North Carolina | — |
Countries
Brazil
Contacts
Public ContactLaura Gonçalves
Universidade de São Paulo
Outcome results
None listed