Comparison between different methods of root canal treatment in children.

Not Applicable

Recruiting

• Conditions: Pulpitis, dental pulp necrosis; C07.793.237.820; C07.793.237.315

• Registration Number: RBR-58m7f6
• Lead Sponsor: Faculdade de Odontologia da Universidade Federal do Rio de Janeiro

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-04-06
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

Posterior teeth with deep caries lesions and associated interradicular and / or periapical radiolucency; teeth affected by caries with abnormal mobility due to periapical pathology, but not associated with physiological exfoliation; history of spontaneous pain; teeth presenting intraoral swelling or drainage of the sinus tract; continuous bleeding after amputation of the coronal pulp tissue; and teeth with external physiological or pathological resorption involving less than a third of the root length.

Exclusion Criteria

Systemic pathology (clinically compromising conditions and special health care needs); history of allergic reaction to local anesthetics or to the components of the test materials; antibiotic therapy in the 30 days prior to the intervention or during treatment; teeth unable to receive absolute isolation and / or unable to be restored; tooth that has previously undergone root canal manipulation; tooth with interradicular or periapical radiolucency involving more than half of the smallest vertically measured root; tooth with internal root resorption; tooth with physiological or pathological external root resorption of more than one third of its length; root canal obliteration; or inadequate bone support evidenced by non-physiological tooth mobility compared to the contralateral tooth.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Similar clinical and radiographic success rates for both methods employed, verified through clinical and radiographic examinations performed every 6 months, to be submitted to statistical analysis.

Secondary Outcome Measures

Name	Time	Method
Secondary outcomes are not expected.