Type II diabetes mellitus
Conditions
Interventions
The randomization of patients in relation to the treatment group will be performed by drawing lots with numbered opaque envelopes. Randomization will be performed by another study author. Participants
Sponsors
Universidade Federal de Minas Gerais
Universidade Federal de Minas Gerais
Eligibility
Age
30 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with type II diabetes mellitus; patients with periodontitis stage II or III; minimum age of 30 years; at least fourteen teeth in the mouth
Exclusion criteria
Exclusion criteria: Individuals with diseases with alteration in the immune system; smokers; individuals who make use of dietary supplementation; individuals who need a diet with low sodium concentrations; pregnant and lactating women; individuals who have undergone periodontal treatment in the last 6 months; individuals with implants and peri-implant diseases; individuals who have undergone antimicrobial and anti-inflammatory therapy in the last 3 months; Individuals who have renal dysfunction; individuals who use anticoagulants and antiplatelet agents; individuals who changed their diabetes medication during the study period; individuals using insulin; Individuals with glycated hemoglobin above 9%; individuals with fasting blood glucose above 250mg/dl
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate the average probing depth. The probing depth, distance from the gingival margin to the bottom of the sulcus or periodontal pocket, will be evaluated with millimeter periodontal soda in the four sites (mesial, buccal, distal and lingual/palatine) of all present teeth. The probing depth will be recorded in millimeters and the average will be calculated for each individual considering the number of teeth and sites present. Probing depth will be assessed before the intervention and 60 and 90 days after the intervention. A greater reduction in mean probing depth is expected in the test group after intervention compared to the control group. a difference of 1mm in mean probing depth between groups is considered significant. | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate bleeding on probing. Bleeding on probing will be evaluated with millimeter periodontal soda in the four sites (mesial, buccal, distal and lingual/palatal) of all present teeth. Bleeding on probing will be recorded as present or absent and the average will be calculated for each individual considering the number of teeth and sites present. Probing bleeding will be assessed before the intervention and 60 and 90 days after the intervention. A greater reduction in mean probing bleeding is expected in the test group after intervention compared to the control group. | — |
Countries
BR
Contacts
Public ContactPierre
Universidade Federal de Minas Gerais
Outcome results
None listed