Surgery, Oral
Conditions
Interventions
Low intensity laser will be applied in half of the sample (n=8), test group and the placebo laser in another half (n=8), control group. The laser used will be the Laser Duo MMOptics, which will be app
E02.594.540
Sponsors
Faculdade de Odontologia da Universidade Federal de Minas Gerais
Faculdade de Odontologia da Universidade Federal de Minas Gerais
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients over 18 years; periodontal health; to sign of the Declaration of Consent; to present from sites with bleeding to approval of less than 10%.
Exclusion criteria
Exclusion criteria: Individuals who are diabetic; pregnant and lactating; in need of prophylaxis for bacterial endocarditis; using analgesic or anti-inflammatory medication; smokers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative pain, determined through the pain scale (0-10), in the first seven days after surgery. Pain reduction is expected in the test group. | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of epithelialization - Test with hydrogen peroxide at 4, 7 and 14 days after surgery. Faster epithelialization is expected in the test group. ;Bleeding - Clinical evaluation at 1,2,3,4 days after surgery. Decreased bleeding is expected in the test group.;Edema- Clinical evaluation at 1,2,3,4 days after surgery. Decrease in edema is expected in the test group. | — |
Countries
Brazil
Contacts
Public ContactBárbara Freire
Faculdade de Odontologia da Universidade Federal de Minas Gerais
Outcome results
None listed