Chronic Apical Periodontitis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Any individual presenting with posterior teeth with a clinical picture of pulp necrosis and radiographic evidence of apical periodontitis, presenting lesions greater than 2 mm in diameter;Agree to participate and sign the informed consent form
Exclusion criteria
Exclusion criteria: Teeth with great coronary destruction, requiring prosthetic rehabilitation; Present any pre-existing general and / or oral clinical condition that puts the individual at risk during the study; Being pregnant or breastfeeding; Patient with generalized periodontal disease or affecting the tooth that needs endodontic treatment; Allergic reaction to chemicals used in endodontic treatment;Teeth that do not present complete root formation - incomplete rhizogenesis; Teeth that present radiographic evidence of internal or external root resorption; Teeth whose root canal is calcified; Teeth submitted to previous endodontic treatment; History of antibiotic use prior to treatment; or need for antibiotic prophylaxis (eg bacterial endocarditis); Teeth that present vital pulp tissue, even if radiographically there is presence of radiolucent image associated with the periápice; Teeth that, during the endodontic treatment, show signs of root fracture; When, during the endodontic procedure, accidents and complications occur, specifically root perforations and instrument separation within the SCR; Patients who do not return to reassessment appointments
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Expected Outcome 1: Changes in the PAI index 6 months after treatment; verified by means of periapical index scores attributed to each tooth in the periapical radiographs at each of the evaluation times; from the comparison of the mean values of the scores between the evaluation times;Expected Outcome 2: Radiographic quality of endodontic obturation; verified by periapical radiographs after completion of the treatment, taking into account the parameters apical extension, homogeneity and conicity; from the proportion of endodontic obturations classified as "perfect"; "satisfactory" and "deficient";Expected Outcome 3:Incidence of postoperative pain and its severity at 24, 48, 72 hours and 7 days; verified by means of verbal scale (incidence) and visual analogue scale (severity) from the proportion of patients who affirm that postoperative sensitivity has occurred and the calculation of mean severity indicated in the visual analogue scale | — |
Primary
| Measure | Time frame |
|---|---|
| Change in periapical index (PAI) 12 months after treatment; verified by means of periapical index scores attributed to each tooth in the periapical radiographs at each of the evaluation times; from the comparison of the mean values of the scores between the evaluation times | — |
Countries
Brazil
Contacts
Universidade Federal de Sergipe;Universidade Federal de Sergipe