Pulp necrosis
Conditions
Interventions
This is a two-arm, double-blind, randomized controlled clinical trial. Experimental group: 77 patients with mandibular molars diagnosed with pulp necrosis and periapical lesion will receive endodontic
E06.397
Sponsors
Universidade Federal de Santa Catarina
Universidade Federal de Santa Catarina
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients: healthy (ASA I classification); over 18 years of age; asymptomatic; indication for endodontic treatment of manbidular molar (first or second). Dental element: pulp necrosis; negative response to the cold pulp sensitivity test; radiographic image compatible with a radiolucent periapical lesion of origin endodontic.
Exclusion criteria
Exclusion criteria: Patients: who have some type of comorbidity; smokers; pregnant; under 18 years old; who have used medication that may alter the perception pain, such as analgesics or anti-inflammatory, at least 48 hours before the procedure, and use of antibiotics 30 days before treatment. Dental element: prior manipulation of root canals; associated periodontal lesion; interradicular furcation lesion; mobility above grade I; presence of fistula, abscess or edema; calcified or internally resorbed root canals; roots with a degree of curvature greater than 45 degrees; incomplete root formation; C shaped internal anatomical conformation; widely destroyed crown that makes absolute isolation and/or restoration impossible immediate finish with composite resin.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find a 10% difference in the comparison of success rates between the control and intervention groups after 12 months of follow-up. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find no difference in the prevalence (% patients who had postoperative pain) and in the intensity of postoperative pain between the control and intervention groups, at the following times: 2h, 12h, 24h, 48h, 72h and 7 days after endodontic treatment. | — |
Countries
Brazil
Contacts
Public ContactFilipe Vitali
Universidade Federal de Santa Catarina
Outcome results
None listed