Anomalies of tooth position Unerupted and Impacted Teeth
Conditions
Interventions
This is a randomized, double-blind clinical study. Eligible participants will be randomly assigned to groups using a list of random numbers generated in Microsoft Excel® via the "
randbetween"
function. Experimental Group I: 16 healthy patients (ASA I) of both sexes, aged 18 to 35, requiring the removal of both mandibular third molars, with the use of aromatherapy (lavender essential oil) d
rescue medication usage during the first postoperative week will also be quantified. Quality of life will be assessed using the "
Oral Health Impact Profile-14"
(OHIP-14) questionnaire at the initial consultation, 24 hours after the procedure, and 7 days after the procedure.
Sponsors
Centro Universitário Christus - UNICHRISTUS
Centro Universitário Christus - UNICHRISTUS
Eligibility
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Healthy individuals classified as ASA I by the American Society of Anesthesiologists; of either sex; aged 18 to 35 years; requiring the removal of both lower third molars; with unerupted mandibular third molars; and with third molars showing similar patterns of root formation, position, and degree of impaction on the right and left sides of each volunteer, as observed on panoramic radiographs
Exclusion criteria
Exclusion criteria: The following will be excluded: smokers; pregnant or lactating women; individuals with orthodontic bands on the mandibular second molars; those showing signs of any preoperative inflammatory or infectious condition; and patients with systemic diseases, neurological disorders, or hearing loss/auditory disorders related to sound interpretation that could influence the study results
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: Mean differences are expected in clinical parameters related to pain, assessed using the visual analog scale.;Outcome 1: It was observed that postoperative pain peaked at 2 hours and decreased after 4 hours in all groups, with more sustained relief observed in the lavender and orange groups. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 2: Mean differences are expected to be found in clinical parameters related to the impact on quality of life, assessed via the “Oral Health Impact Profile-14” (OHIP-14) questionnaire, which focuses primarily on negative effects.;Outcome 2: It was observed that only the lavender group showed a significant increase in scores after 7 days (p=0.008). | — |
Countries
BR
Contacts
Public ContactEdson Cetira Filho
Centro Universitário Christus - UNICHRISTUS
Outcome results
None listed