Pulpitis
Conditions
Interventions
This is a pragmatic randomized clinical trial, two arms, double-blind, where the 134 patients will be randomized using the block technique and stratified by sex. A double-blind design will be used, wh
E06.397.778
Sponsors
Faculdade de Odontologia da Universidade Federal do Amazonas
Universidade Federal do Amazonas (UFAM)
Eligibility
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Competent adult patients; both genders; aged between 18 to 65 years; with referral for endodontic treatment in permanent teeth from public healthcare services with referral documentation; patients with contact number
Exclusion criteria
Exclusion criteria: Patients at any gestational stage; immunocompromised or with special needs; teeth presenting endodontic complications; teeth with calcifications; teeth with external or internal resorptions; incomplete root formation; teeth with dental perforations; teeth with longitudinal or vertical fractures; severe periodontal disease; teeth not completed in a single session
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the occurrence and intensity of post-endodontic pain by applying a numerical rating scale ranging from zero (no pain) to 10 cm (maximum pain) in research participants at 24, 48, and 72 hours after endodontic treatment | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find a lower occurrence and intensity of postoperative pain in the intervention group, with a difference of 30% between the groups | — |
Countries
Brazil
Contacts
Public ContactEmilio Sponchiado
Universidade Federal do Amazonas (UFAM)
Outcome results
None listed