search
Back to results

Endodontic Treatment of Primary Teeth With Guedes-Pinto Paste Without Antibiotic

Primary Purpose

Pulp Disorder

Status
Completed
Phase
Phase 3
Locations
Brazil
Study Type
Interventional
Intervention
Endodontic treatment using Guedes-Pinto Paste
Endodontic using Guedes-Pinto Paste without antibiotic
Sponsored by
University of Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulp Disorder focused on measuring pulpectomy, primary teeth, root canal filling materials

Eligibility Criteria

4 Years - 8 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Primary molar teeth with necessity of endodontic treatment.
  • Patients whose parents or guardians consent to their participation in the study

Exclusion Criteria:

  • Systemic health problems, congenital facial deformities, facial tumors or syndromes
  • Teeth presenting one of the following:

    • Resorption of more than 2/3 of the root
    • Destruction of the crypt of the permanent successor
    • Pulp chamber floor drilling.
    • Presence of internal resorption

Sites / Locations

  • School of Dentistry, University of Sao Paulo

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Pasta Guedes-Pinto

Pasta Guedes-Pinto without antibiotic

Arm Description

Endodontic treatment using Guedes-Pinto Paste

Endodontic using Guedes-Pinto paste without antibiotic

Outcomes

Primary Outcome Measures

Success or failure of treatment
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: no occurrence of a periapical rarefaction in the furcation area; reduction or maintenance of an already present bone rarefaction in the furcation area of posterior teeth, 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, we will compare the initial and final radiographs.

Secondary Outcome Measures

Full Information

First Posted
February 11, 2019
Last Updated
April 17, 2021
Sponsor
University of Sao Paulo
search

1. Study Identification

Unique Protocol Identification Number
NCT03839485
Brief Title
Endodontic Treatment of Primary Teeth With Guedes-Pinto Paste Without Antibiotic
Official Title
Endodontic Treatment of Primary Teeth With Guedes-Pinto Paste Without Antibiotic: Randomized Non-inferiority Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
June 8, 2018 (Actual)
Primary Completion Date
June 30, 2019 (Actual)
Study Completion Date
April 10, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The pulp therapy in primary teeth is still necessary even with all odontopediatrics evolution in prevention and minimal intervention, aiming to keep the tooth free of inflammation or infection and in a functional state until its exfoliation. Several materials are used as filling paste of primary teeth. In Brazil, the Guedes-Pinto Paste (PGP), an association of iodofórmio, camphorated paramonochlorophenol, prednisolone and rifamycin, has been widely used for some decades. However, current Brazilian legislation has made it difficult to commercialize antibiotics, which has made it difficult to obtain the ointment that is the association between prednisolone and rifamycin. Therefore, the objective of this clinical trial will be to test PGP without rifamycin in the pulpectomy of primary teeth, and to compare it with the treatment performed with conventional PGP.
Detailed Description
A randomized triple-blind non-inferiority clinical study with two parallel arms, with a 12-month follow-up, will be performed. The experimental group will be PGP formulated without the antibiotic, while the control group is the conventional PGP, containing rifamycin. The conventional pulpectomy will be performed using manual files, performing the instrumentation aided by Endo-PTC and 1% sodium hypochlorite. At the end of the instrumentation, just before the obturation, the groups will be drawn, with the strategy of randomization in permuted blocks and stratified by the initial condition of the tooth (with or without periapical lesion). The main outcome will be the clinical and radiographic success of endodontic treatment after 12 months.Patients who seek the dental service of the municipality and require endodontic treatment will be invited to participate in the study. The data will be statistically analyzed using the statistical package Stata 12.0 (Stata Corporation, College Station, TX, USA). The longevity of the treatments will be evaluated by estimating survival rates using the Kaplan-Meier method. The differences between survival rates according to the type of endodontic treatment proposed will be analyzed through the Log-rank test.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulp Disorder
Keywords
pulpectomy, primary teeth, root canal filling materials

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Masking Description
Both materials will be packed in identical and opaque syringes, identified only with letters (A and B). The codes will be revealed only at the end of the study. Neither the professional who will be performing the treatment, nor the patient or the evaluator, who will perform the exams at follow-up times, will know which of the two materials of choice were selected for each tooth, characterizing the study as triple-blind.
Allocation
Randomized
Enrollment
98 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pasta Guedes-Pinto
Arm Type
Active Comparator
Arm Description
Endodontic treatment using Guedes-Pinto Paste
Arm Title
Pasta Guedes-Pinto without antibiotic
Arm Type
Experimental
Arm Description
Endodontic using Guedes-Pinto paste without antibiotic
Intervention Type
Drug
Intervention Name(s)
Endodontic treatment using Guedes-Pinto Paste
Other Intervention Name(s)
Pulpectomy with Guedes-Pinto paste
Intervention Description
Dental procedure in which the entire pulp chamber is removed from the crown and roots of a tooth and the root filling material Guedes-Pinto paste is applied
Intervention Type
Drug
Intervention Name(s)
Endodontic using Guedes-Pinto Paste without antibiotic
Other Intervention Name(s)
Pulpectomy with Guedes-Pinto paste without antibiotic
Intervention Description
Dental procedure in which the entire pulp chamber is removed from the crown and roots of a tooth and the root filling material Guedes-Pinto paste without antibiotic is applied
Primary Outcome Measure Information:
Title
Success or failure of treatment
Description
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: no occurrence of a periapical rarefaction in the furcation area; reduction or maintenance of an already present bone rarefaction in the furcation area of posterior teeth, 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, we will compare the initial and final radiographs.
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
8 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Primary molar teeth with necessity of endodontic treatment. Patients whose parents or guardians consent to their participation in the study Exclusion Criteria: Systemic health problems, congenital facial deformities, facial tumors or syndromes Teeth presenting one of the following: Resorption of more than 2/3 of the root Destruction of the crypt of the permanent successor Pulp chamber floor drilling. Presence of internal resorption
Facility Information:
Facility Name
School of Dentistry, University of Sao Paulo
City
Sao Paulo
ZIP/Postal Code
05508-000
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Endodontic Treatment of Primary Teeth With Guedes-Pinto Paste Without Antibiotic

We'll reach out to this number within 24 hrs