Gingival hyperplasia
Conditions
Interventions
Surgery to remove inflammatory fibrous hyperplasia lesion will be performed as an intervention. One group using the diode surgical laser and another using electrocautery with 20 participants each grou
Procedure/surgery
E02.594
K06.2
K06.1
Sponsors
Universidade federal de Minas Gerais
Universidade federal de Minas Gerais
Eligibility
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: Healthy volunteers; age greater than 18 years; both genders; with clinical diagnosis inflammatory fibrous hyperplasia.
Exclusion criteria
Exclusion criteria: Volunteers using analgesic medication; with systemic diseases.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of the efficacy and safety of surgical diode laser with electrocautery in the treatment of inflammatory fibrous hyperplasia, evaluated by the following parameters: postoperative bleeding (according to the indexes: absent, discrete, moderate and intense, the amount of anesthesia used, edema and postoperative pain (visual analogue scale), tissue healing (measurement of the healed area and / or scarring). According to scientific literature, both treatments presents 100% of lesion resolution, and will be observated for 4 weeks postoperative. Lesions with several sizes present the same treatment efficacy and safety. From the statistical analysis, it will be possible to verify if there are differences in postoperative surgical characteristics, as well as the most effective and safe technique for the treatment of inflammatory fibrous hyperplasia. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected. | — |
Countries
Brazil
Contacts
Public ContactRicardo Mesqita
Faculdade de Odontologia da Universidade Federal de Minas Gerais
Outcome results
None listed