se of LED therapy in the control of postoperative symptoms in extractions of impacted third molars

Phase 1

• Conditions: Impacted teeth; K00-K93

• Registration Number: RBR-7kv76vh
• Lead Sponsor: Faculdade de Odontologia da Universidade de São Paulo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-12-15
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

Healthy patients of both gender, aged between 16 and 35 years, who need extraction of both inferior third molars and that these teeth have similar bone impactions bilaterally, observed by means of panoramic radiography, presenting the same classification of dental impaction of according to Pell & Gregory (1933) and Winter (1926).

Exclusion Criteria

Pre or postoperative sensory changes; Use of analgesics or antiinflammatory drugs in the 48 hours prior to extractions; Pregnant or lactating women; Known hypersensitivity to any of the drugs used in the study (Mepivacaine, Amoxicillin, Ibuprofen, Dipyrone, Chlorhexidine); Patients with postoperative infections or alveolitis; Failure to follow postoperative recommendations; Failure to attend postoperative consultations; Technical failure in anesthesia or need to use more than three anesthetic tubes; Surgeries with operative time greater than 40 minutes; Patients with temporomandibular joint dysfunction or limited mouth opening; Individuals who do not have the upper and lower central incisors.

Study & Design

• Study Type: Intervention
• Study Design: Not specified