Pulpitis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Be in good health; Be in the age group over 18 years; Present a clinical diagnosis of symptomatic pulpitis in posterior lower teeth; Ability to understand the pain assessment scale
Exclusion criteria
Exclusion criteria: Under 18 years old; pregnant women; Patients who have a previous sensitivity, allergy or who cannot take ibuprofen for any other reason; Patients allergic to local anesthetics or sulfites; Patients who have an important history of health problems; Patients unable to give informed consent; Patients who have ingested analgesics or anti-inflammatory drugs in the last 8 hours prior to treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: Increased efficacy of anesthetic blockade of the inferior alveolar nerve, verified upon previous administration of arginine ibuprofen for endodontic treatment in patients with symptomatic pulpitis.;Outcome found 1: In the present investigation, preemptive medication with ibuprofen-arginine provided a rate of 78.0% of efficient blockade of the inferior alveolar nerve and of 62.0% when conventional ibuprofen was used. Despite the results of the ibuprofen-arginine association showing higher values, there was no statistical difference between the two groups in terms of blockade efficiency. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected | — |
Countries
Brazil
Contacts
Faculdade de Odontologia da Universidade Federal de Goiás