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

Randomized clinical assay of use the Mta in Pulpar Therapy of deciduous teeth

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9chxvg
Enrollment
Unknown
Registered
2019-06-17
Start date
2018-02-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Necrosis of pulp

Interventions

It will be performed randomly in the experimental and control groups, treatments of pulpectomy in upper and lower incisors and lower primary molars with two types of drugs, Aggregate mineral trioxide
Procedure/surgery

Sponsors

Angelus Industria de Produtos Odontológicos S/A
Lead Sponsor
Universidade Estadual Paulista "Júlio de Mesquita Filho"
Collaborator

Eligibility

Age
2 Years to 12 Years

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
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. ;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.

Secondary

MeasureTime frame
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.

Countries

Brazil

Contacts

Public ContactCássia;Robson Dezan - Garbelini;Cunha

CCS - COU - Programa de Pós-Graduação em Odontologia;Universidade Estadual Paulista "Júlio de Mesquita Filho"

dgcassia@gmail.com;robson.cunha@unesp.br+554333239455;+551836363200

Outcome results

None listed

Source: REBEC (via WHO ICTRP)