Efficacy of dental anesthesia in retromolar canal.

Not Applicable

Recruiting

• Conditions: Pacients with gingivitis; Dental caries.; C07.465.714.258.480; C07.793.720.210

• Registration Number: RBR-4sntgt
• Lead Sponsor: Faculdade de odontologia de Ribeirão Preto

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-05-02
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

retromolar presence;needed inferior alveolar nerve anesthesia

Exclusion Criteria

jaw bone lesions;oral mucosal lesions;lidocaine allergy 3%

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Presentation of expected outcome: tactile and tactile pain response; Method used for ouctome: pressure with Florida Probe (25g force and 2mm of insercion) and pulpal pain response with Roeko Endo Frost (5 seconds on vestibular of tooth in question); <br>The parameters to mesure will be provided by the patient by him/herself using a pain scale (visual and analog) with the value of zero to 10 (no pain and maximum pain). To verify if the outcome has actually occurred, the specific timing of the measurement will be made 5 minutes after the application of dental anesthesia.

Secondary Outcome Measures

Name	Time	Method
Secondary outcomes are not expected.