Pulpitis
Conditions
Interventions
Experimental group: 50 healthy adults with pulpitis in permanent molars will undergo endodontic treatment with a reciprocating system in a single visit and the sealer used will be based on calcium sil
E06.397.778
Sponsors
Universidade Federal do Amazonas
Universidade Federal do Amazonas
Eligibility
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Men and women aged 18–65 years, diagnosed with symptomatic irreversible pulpitis with indication for endodontic treatment in permanent molar teeth, will be included in the study, confirmed by positive response to clinical, cold vitality and radiographic tests. The individual who participates in this research must have a contact number (phone or cell phone) to be able to carry out the post-operative evaluations.
Exclusion criteria
Exclusion criteria: Patients who were pregnant, immunocompromised, on medication or hypersensitive to anti-inflammatory drugs, or patients with occlusal disorders or any type of periodontitis or endodontic complications were excluded from the study, since these conditions would interfere with the analysis of the presence of pain after endodontic treatment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the prevalence of postoperative pain after endodontic treatment in patients participating in the research in a period of 6, 12, 24, 48 and 72 hours and its intensity using a validated pain scale NRS type with a score of zero (no pain) up to 10 cm (maximum pain). | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcomes will be worked with the statistical analysis of regression to verify if the occurrence of postoperative pain of the primary outcome could be being influenced by the possible accidental cases of overfilling or by the need of administration of rescue medication among the participants of the groups. | — |
Countries
Brazil
Contacts
Public ContactEmílio Sponchiado Junior
Universidade Federal do Amazonas
Outcome results
None listed