Pericoronitis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participants with signs/symptoms of pericoronaritis, such as the occurrence of spontaneous pain, erythema, purulent or draining edema, affecting the gingiva of the oral cavity, located over the lower third molar; age 18 to 35 years; both sexes; surgical risk level I and level II, according to the American Society of Anesthesiologists (ASA I and ASA II); periodontal status level I and II, according to the American Academy of Periodontology; consent to participate in this clinical trial by signing the Informed Consent Form (ICF)
Exclusion criteria
Exclusion criteria: Participants with surgical risk level III and level IV, according to the American Society of Anesthesiologists (ASA III and ASA IV); with periodontal status level IV, according to the American Academy of Periodontology; undergoing antibiotic therapy in the last two months; with any medical contraindication for periodontal probing; currently using tobacco and aged less than 18 years and more than 35 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| We expect to find a difference in the level of pain and quality of life | — |
Secondary
| Measure | Time frame |
|---|---|
| A reduction in probing depth and recovery of the bone crest level in the distal second molar, greater mouth opening and less edema/erythema measured by the diameter of the lesion are expected | — |
Countries
Brazil
Contacts
Universidade Federal dos Vales do Jequitinhonha e MucurI