A randomized clinical study using Mta for the treatment of canal on milk teeth

Not Applicable

Recruiting

• Conditions: ecrosis of pulp; Pulpitis; Periapical Abscess; C07.793.237.315; C07.793.237.820; C01.539.830.025.650

• Registration Number: RBR-9chxvg
• Lead Sponsor: Angelus Industria de Produtos Odontológicos S/A

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-06-17
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

Healthy children;upper and lower incisors or deciduous lower molars with deep carious lesion reaching the root pulp;spontaneous and persistent pain, dark red bleeding of difficult control; maximum resorption up to 2/3 of the root;restorable tooth;pulp exposure with clinical evidence of necrotic pulp or irreversible pulpitis.

Exclusion Criteria

Upper and lower incisors or deciduous lower molars with internal resorption;fistula near the gingival margin;Pulmonary calcifications; pathological mobility;periapical bone rarefaction with evidence of continuity solution in the crypt of the permanent successor germ.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Expected outcome 1, Absence of pain, verified by pre and post-intervention dental clinical examination.;Expected outcome 2, Absence of edema within a period of up to two years, verified by pre and post-intervention dental clinical examination.;Expected outcome 3, Absence of abscess in the period up to two years, verified by pre and post-intervention dental clinical examination.;Expected outcome 4, Absence of fistula within a period of up to two years, verified by pre and post-intervention dental clinical examination.;Expected outcome 5, absence of pathological mobility in the period of up to two years, verified by pre and post-intervention dental clinical examination.<br>;Expected outcome 6, Absence of diffuse or surrounding bone rarefaction and pathological root resorption (internal or external) in the two-year period, verified by pre and post-intervention dental radiography.<br>

Secondary Outcome Measures

Name	Time	Method
Expected outcome 1, Presence of physiological root resorption without interference of the obturator material in the two-year period, verified by pre and post-intervention dental radiographic examination.<br>