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Pulpectomy in primary teeth: randomized controlled clinical trial evaluation

Pulpectomy in primary teeth: randomized controlled clinical trial evaluation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-8ngvnn
Enrollment
Unknown
Registered
2016-01-05
Start date
2014-08-25
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

pulpitis, pulp necrosis

Interventions

Children with teeth presenting periapical or furcation injury will be selected to receive endodontic treatment. Procedures will be carried out according to a standard clinical protocol previously esta
Group 2-Modified Guedes-Pinto paste (Nebacetin, PMCC and iodoform)
Group 3- Calcium hydroxide paste (Calcium hydroxide P.A., propylene glycol and zinc oxide). Clinical and radiographic data will be analyzed at 30, 60, 90 days, 6 months, 1 year and 2 years after treat
Procedure/surgery
Radiation
E06.397

Sponsors

Universidade Federal de Santa Maria
Lead Sponsor
Universidade Federal de Santa Maria
Collaborator

Eligibility

Age
2 Years to 9 Years

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Brazil

Contacts

Public ContactMarta Dutra Machado Oliveira

Universidade Federal de Santa Maria

marta@ufsm.br+55 55 3222-9428

Outcome results

None listed

Source: REBEC (via WHO ICTRP)