ow-level laser effect on the tooth root treatment

Not Applicable

Recruiting

• Conditions: Pulpitis; K04.0

• Registration Number: RBR-5smzhp
• Lead Sponsor: niversidade Federal do Amazonas (UFAM)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-01-06
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

Adult patients; with endodontic treatment indication in permanent lower molars; diagnosed with irreversible pulpitis; have contact number to be able to perform the postoperative evaluations

Exclusion Criteria

Pregnant patients; administering any medication when treatment; immunocompromised; with hypersensitivity to non-steroidal anti-inflammatory drugs; patients who have teeth with endodontic complications (calcifications, external or internal resorption, partial formation of apical summit with dental drilling, with longitudinal or vertical fractures and severe periodontal disease); patients who can not have endodontic treatment completed in the same session; Patients who for any reason can not be contacted by phone for the evaluation of pain after endodontic treatment.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Presence or absence of postoperative pain after endodontic treatment using Waveone system and applying photobiomodulation therapy, which will be verified by two scores measuring pain, numerical and verbal description, a reduction of 30% of expected pain after endodontic treatment using only the Waveone system and outcomes will be presented by percentage

Secondary Outcome Measures

Name	Time	Method
Influence of predictor variables (age, sex, tooth, prior dentin sensitivity) on the primary outcome variable of pain after endodontic treatment, verified by history taken before performing the treatment