eedle-less anesthesia compared to conventional: clinical trial

Phase 3

• Conditions: Impacted teeth. Unerupted tooth. Tooth, Impacted. Third molar. Tooth, Unerupted.; A14.549.167.860.525.500; C07.793.905; K01.1; K01.0; A14.549.167.860.715

• Registration Number: RBR-9qm2y5
• Lead Sponsor: CESMAC- Centro de Ensino Superior Maceió

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-01-09
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

Patients of both genders, systemically healthy, aged between 18 and 45 years and need to remove the contralateral third molars, which were in symmetrical position.

Exclusion Criteria

Patients with a history of anesthesia or vasoconstrictor allergy employed, with third molars in non-symmetrical position or who had used anti-inflammatory, analgesic or antidepressant prior to surgery.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Expected outcome 1<br>Pain score reduction, verified through the visual analogue pain scale, after finding a variation of at least 1 mm after the anesthesia procedure.;Expected outcome 2<br>Vital sign changes before and after infiltration of anesthetic solutions using both devices. These should be verified by comparing blood pressure, pulse and respiratory rate, based on the finding of variation between their means,<br>before and after anesthetic solution infiltration. ;Expected outcome 3<br>Patient satisfaction level, verified through a questionnaire made available to the patient after anesthesia, to be completed according to a Likert scale, based on the finding of variation of at least 1 point of the score for each question.

Secondary Outcome Measures

Name	Time	Method
o Secondary Outcomes Expected.