Evaluation of use of tissue adhesive in surgeries of wisdom tooth

Not Applicable

• Conditions: Wound Healing; E04.545

• Registration Number: RBR-108mccss
• Lead Sponsor: niversidade Federal do Paraná

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2023-09-10
• Study Start: 2023-11-21
• Last Update Posted: 19 December 2023

Recruitment & Eligibility

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

Inclusion Criteria

Adult individuals of both sexes; Presence of bilateral mandibular third molars in similar positions, according to Winter's classification; Agree to participate in the study

Exclusion Criteria

Allergy to any component of Dermabond®; Patients using medications that may interfere with healing (antiplatelet agents, anticoagulants, immunosuppressants, corticoids); Smoking patients; Patients with uncontrolled systemic alterations

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
It is expected to find no difference in healing, postoperative pain, edema and bleeding between the cyanoacrylate tissue adhesive (Dermabond®), evaluated through postoperative questionnaires and facial measurements

Secondary Outcome Measures

Name	Time	Method
o secondary outcomes are expected