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Clinical Trials/NCT02216942
NCT02216942
Completed
Phase 3

Endodontic Treatment of Primary Teeth With Guedes Pinto Paste: A Randomized Clinical Trial

Fausto Medeiros Mendes1 site in 1 country104 target enrollmentJanuary 2015

Overview

Phase
Phase 3
Intervention
Endodontic treatment using Vitapex
Conditions
Endodontic Treatment of Primary Teeth
Sponsor
Fausto Medeiros Mendes
Enrollment
104
Locations
1
Primary Endpoint
Success or failure of two endodontic treatments
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The maintenance of primary teeth until their exfoliation has been one of the main purposes of Pediatric Dentistry, are they representing the fundamental basis for proper occlusion of the permanent dentition. Often, injuries or extensive dental caries reach the pulp of deciduous teeth making maintenance on these dependent endodontic treatment arc. Thus, this study was to conduct a randomized clinical trial with longitudinal follow-up of two years, double blind, to compare the degree of success of endodontic treatment in primary among the most used folder, Guedes Pinto paste, and one Calcium hydroxide and iodoform paste to control, Vitapex.

Detailed Description

After approval by the ethics committee of the patients Faculty of Dentistry, University of São Paulo that having root canal filling of primary teeth will be invited to participate in the study. A clinical examination and prior radiographic diagnosis and also a quality of life questionnaire regarding oral health (- ECOHIS Early Childhood Oral Health Impact Scale) will be-held. The patient will be randomized to one of two groups and will be held endodontics by a blind handler. The patient will be accompanied with periods of one week, six months, 12 months and 24 months by a blinded evaluator. At the last visit of the review ECOHIS questionnaire will be reapplied to those responsible. The outcome will be the success or failure of endodontic treatments evaluated through permanent tooth in the arch on clinical and radiographic conditions of normality. The longevity of the treatments will be evaluated by estimating survival rates by Kaplan-Meier. The differences between the survival rates according to the type of proposed endodontic treatment will be analyzed using the log-rank test with a minimum significance level of 5%.

Registry
clinicaltrials.gov
Start Date
January 2015
End Date
February 2018
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Fausto Medeiros Mendes
Responsible Party
Sponsor Investigator
Principal Investigator

Fausto Medeiros Mendes

Fausto Medeiros Mendes

University of Sao Paulo

Eligibility Criteria

Inclusion Criteria

  • Primary teeth with pulp diagnosis and need endodontic treatment
  • Patients whose guardians consent to their participation in the survey
  • fistula or abscess
  • bone rarefaction or visual diagnosis
  • teeth in the remaining tooth structure and location of the injury rehabilitation permit
  • do not have internal or external resorption involving more than one third of the root length
  • have no bone loss in lateral root and disruption crypt and the presence of at least half of root

Exclusion Criteria

  • health problems systemic
  • congenital facial deformities
  • facial tumors
  • syndromes

Arms & Interventions

Vitapex

Endodontic treatment using Vitapex

Intervention: Endodontic treatment using Vitapex

Guedes Pinto Paste

Endodontic treatment using Guedes Pinto

Intervention: Endodontic treatment using Guedes Pinto

Outcomes

Primary Outcomes

Success or failure of two endodontic treatments

Time Frame: two years

The success or failure of endodontic treatments evaluated by the time spent in the tooth arch in clinical conditions of normality. Clinical criteria for determining success are: absence of fistula, absence of painful symptoms and pathological absence of adequate mobility and gingival contour. Radiographically, the success criteria are: absence / reduction of periapical bone rarefaction in anterior and absence / bone rarefaction in the furcation area of later, maintaining the periradicular space, root resorption compatible with the eruptive phase and absence of pathological bone resorption. To evaluate the reduction of lesions or appearance of new lesions will be between the initial and follow-up radiographs. Radiographs will be scanned and the end of the bone rarefactions starting area and will be measured on a software image analysis.

Secondary Outcomes

  • Quality of the obturation obtained with the two root canal filling pastes(two years)

Study Sites (1)

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