se of topical anesthetic before and after third molar removal surgery

Not Applicable

• Conditions: Acute pain; Pain, Postoperative; C23.888.592.612

• Registration Number: RBR-6s82bk3
• Lead Sponsor: Centro Universitário Christus - UNICHRISTUS

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-12-11
• Last Update Posted: 19 December 2023
• Study Completion: 2024-06-30

Recruitment & Eligibility

• Status: Recruitment completed
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Healthy individuals (American Society of Anesthesiologists - ASA I); of both sexes; aged between 18 and 35 years; in need of removal of lower third molars; third molars that present, on panoramic radiography, similar patterns of root formation, position and degree of impaction when comparing the right and left sides of each volunteer

Exclusion Criteria

Smokers; pregnant or breastfeeding women; users of medications prior to surgery that may interact with the patient's pain (e.g. NSAIDs, corticosteroids, analgesics); wearers of orthodontic bands on mandibular second molars; signs of any preoperative inflammatory or infectious condition; systemic diseases; neurological disorders

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Evaluate mean differences in clinical parameters related to inflammatory events (pain). Pain will be assessed using the visual analogue scale,in which a reduction in pain is expected in the intervention group compared to the control group.