Success of Endodontic Treatement of anterior teeth with Reciproc system instruments

Not Applicable

Recruiting

• Conditions: Apical Periodontites; C07.320.830.700

• Registration Number: RBR-7zcp2n
• Lead Sponsor: niversidade Federal de Sergipe

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-09-20
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Volunteers with anterior teeth presenting pulpal necrosis and radiographic evidence of apical periodontites whose diameter is higher than 2mm; that agree to paticipate and sign the informed consent sheet.

Exclusion Criteria

volunteers with teeth that will need crow placement due to advanced destruction; volunteers with a pre-existing health or oral condition that puts him at risk during the trial; pregnant or breast feeding; volunteers with generalized periodontal desease or periodontal desease affecting the tooth to be included; volunteers allergic to any of the substances used during endodontic treatment; volunteers whose elegeble teeth has not completed its root formation, and , therefore, has an open apex; volunteers whose elegeble teeth presents radiogtaphic evidence of internal or external root resorption; volunteers whose elegible teeth has a calcified root canal space or has allready been submitted to root canal treatment; voluntters with a history of antibiotic, anti-inflamatory or analgesic use 15 days before endodontic treatment is to be performed; volunteers who have to have antibiotics prophylaxis due to bacterial endocarditis; volunteers whose elegible tooth has vital pulp tissue, even in the presence of a radiographic lesion; whose elegible teeth shows signs of root fracture during endodontic procedure; when accidents occur during endodontic procedure such as root perforation and file separation; teeth whose procedure can not be completed in a single visit due to incapacity to dry the canal (inflammatory exudate or heavy bleeding); patients that do not return to follow-up evaluations.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Changes in Periapical index (PAI) scores 12 months after root canal treatment; verified through PAI scores attributed to each teeth´s periapical radiography at each of the evaluation times; by the comparison of mean PAI scores values between the evaluation times.