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Influence of Temporary Filling Material Composition on the Success Rate of Endodontic Treatments

NCT03488316 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2018-04-10

No results posted yet for this study

Summary

The aim of this study is through a randomized clinical trial, double blind, splitmouth, evaluate the success rate (contamination rate, periapical lesion relapse and the presence of exudate between the treatment's sessions) of endodontically treated teeth that required filling with temporary material. The composition of the temporary filling material (cement (Based on calcium hydroxide; and based on mineral trioxide aggregate) will be evaluated. Data will be collected, tabulated and submitted to statistical analysis.

Conditions

  • MTA
  • Calcium Hydroxide
  • Endodontic Treatment

Interventions

PROCEDURE

Carie removal

Carie removal with a low speed handpiece

PROCEDURE

Absolute isolation

Absolute isolation with rubber dam

DRUG

Manipulation of the temporary filling material based on Calcium Hydroxide

Manipulation of the temporary material based on Calcium Hydroxide according to the manufacturer's recommendations.

DRUG

Manipulation of the temporary filling material based on Mineral trioxide aggregate

Manipulation of the temporary material based on Mineral trioxide aggregate according to the manufacturer's recommendations.

PROCEDURE

Material insertion on the root canal

Material insertion on the root canal according to the manufacturer's recommendations

PROCEDURE

Material re-insertion on the root canal accordging to the infection needs.

Material re-insertion on the root canal according to the manufacturer's recommendations

PROCEDURE

Definiteve canal root obturation

Definiteve canal root obturation with gutta-percha and definitive cement.

PROCEDURE

Definitve restoration

Definitve restoration confecction.

Sponsors & Collaborators

  • PAULO VINICIUS SOARES

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-01
Primary Completion
2018-07-01
Completion
2019-12-30

Countries

  • Brazil

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03488316 on ClinicalTrials.gov