Pain, postoperative
Conditions
Interventions
This is a two-arm, double-blind, randomized controlled clinical study.TruNatomy Group: 70 patients will receive root canal treatment with the TruNatomy instrument. Xp-endo Shaper Group: 70 patients wi
V03.175.250.500.500
Sponsors
Universidade de Pernambuco
Universidade de Pernambuco
Fundação de Hematologia e Hemoterapia do Estado de Pernambuco
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patient with physical status classified as ASA I (American Society of Anesthesiologist); vital permanent posterior teeth (diagnosis of normal pulp); no symptoms; maxillary or mandibular, premolar or molar; indication of conventional endodontic treatment for prosthetic indication; age 18 or over; both genders
Exclusion criteria
Exclusion criteria: Non-vital teeth; apical periodontitis; endodontic retreatments; symptomatic/asymptomatic irreversible pulpitis; root resorption; teeth with incomplete rhizogenesis; root canal in which the patency of the apical foramen cannot be established; patients who refused to participate in the study; patients in whom the tooth cannot be treated in a single session; patients using any type of medication (analgesics or anti-inflammatories, hormonal or non-hormonal) during the seven days prior to treatment; patients with signs of systemic infection; patients allergic to local anesthetic agents; patients with systemic diseases; decompensated; patients allergic to Sodium Hypochlorite; patients with cognitive impairment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Absence of postoperative pain is expected after intervention with the tested instruments (TruNatomy and Xp-endo Shaper) for root canal treatment.Data collected preoperatively and after treatment at 24h, 48h, 72h and 7 days. | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected. | — |
Countries
Brazil
Contacts
Public ContactDiana De Albuquerque
Universidade de Pernambuco
Outcome results
None listed