Periodontitis
Conditions
Interventions
This is a double-blind, split-mouth randomized clinical study. Experimental group: There will be 23 patients (totaling 46 teeth to be evaluated, 23 test and 23 control) aged over 18 years
Loss of Attachment of 5 mm or more - interproximal teeth not adjacent to lower anterior hemi-arches Non-smokers Non-pregnant Non-lactating Patients who agreed to take part in the research by signing t
E06.721.189.350
Sponsors
Pontifícia Universidade Católica de Campinas
Pontifícia Universidade Católica de Campinas
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients over the age of 18;Insertion Loss of 5 mm or more (Stage III of the New Classification of Periodontal Diseases) - non-adjacent interproximal teeth of hemi-arches lower anteriors; Non-smokers; Non-pregnant women; Non-lactating; Patients who agreed to take part in the research by signing the Term Free and Informed consent
Exclusion criteria
Exclusion criteria: Patients under 18 years of age; That does not present a loss of Insertion of 5 mm or more (Stage III of the New Classification of Periodontal Diseases) - non-adjacent interproximal teeth of lower anterior hemi arches; Smokers; Pregnant women;Nursing mothers; Patients who did not agree to sign the Free and Consent Form Enlightened
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective of the present study is to apply lactobacilli in situ in periodontal pockets, verifying the possible gain in clinical attachment levels and reduction of periodontal pockets. | — |
Secondary
| Measure | Time frame |
|---|---|
| And as a secondary objective, evaluate the time for changes in clinical parameters, if the protocol is effective. | — |
Countries
Brazil
Contacts
Public ContactMônica Celes Campos
Pontifícia Universidade Católica de Campinas
Outcome results
None listed