Pulpitis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
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
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| 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 | — |
Countries
Brazil
Contacts
Universidade Federal do Amazonas (UFAM)