Pulpectomy in primary teeth: randomized controlled clinical trial evaluatio

Not Applicable

Recruiting

• Conditions: pulpitis, pulp necrosis; C07.793.237.820; C07.793.237.315

• Registration Number: RBR-8ngvnn
• Lead Sponsor: niversidade Federal de Santa Maria

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-01-05
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

Eligible patients will be select if they present:primary teeth with at least two years of permanence in mouth; teeth with radiographic changes suggesting apical periodontitis either in root and/or furcation area; cavity that allows restoration with suitable sealing; and teeth without any previous treatment pulp. Patients should have good systemic health, and the data on health history will be recorded.

Exclusion Criteria

Will be excluded from the study: teeth with less than two tears of permanence in the mouth; teeth showing root resorption equivalent to 2/3 or more; presenting radiographic disruption of pericoronal bag of the permanent teeth; primary teeth endodontically treated in a previous session that not present remission of symptoms;teeth with non-appropriate restorative conditions. Patients with any changes to general, are not included in the survey.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Clinical success of the pulpectomies performed in Pediatric Dentistry Clinic of UFSM. Clinical success will be considered when the tooth does not present pain, mobility, fistula or swelling.

Secondary Outcome Measures

Name	Time	Method
Radiographic success of the pulpectomies performed in Pediatric Dentistry Clinic of UFSM. Radiographic success will be considered when reduction in radiolucent aspects corresponding to periapical lesions or furcation previously identified.