pulp necrosis Chronic apical periodontitis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 78 volunteers; male; aged between 18 and 64 years; that already had endodontic treatment indication in permanent molars teeth; diagnosed with necrotic pulp with or without asymptomatic apical periodontitis.
Exclusion criteria
Exclusion criteria: Volunteers at the time of intervention were administering antibiotics or corticosteroids during the treatment; with immunocompromised; which would complicate the systemic disease; these factors could change the perception of pain or interfere with the score analysis of postoperative pain.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected Primary endpoint is the presence of postoperative pain after endodontic treatment in two groups (A Reciproc Technique and B Protaper Technique), the pain presence is evaluated using a VRS scale for periods of 24 72h and 7 days the results will be presented by percentage and applied statistical test is the Mann-Whitney test.;The intensity of pain experienced by patients after endodontic treatment in the Reciproc group was similar to those in the ProTaper group (p > 0.05). In both groups, the highest levels of postoperative pain were recorded 24 h after each procedure, but these levels decreased after 72 h and 7 days after endodon- tic therapy, although differences were not significant (p = 0.55). | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected | — |
Countries
Brazil
Contacts
Faculdade de Odontologia da Universidade Federal do Amazonas;Faculdade de Odontologia da Universidade Federal do Amazonas