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Influence of the Composition of Temporary Restorative Material in Vital Teeth

NCT03437655 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2018-03-07

No results posted yet for this study

Summary

The aim of this study is through a randomized clinical trial, double blind, splithmouth, evaluate the success rate (retation rate and dental sensibility) of temporary direct restorations in vital teeth. The composition of the temporary direct restoration (based on Zinc-Oxide with Eugenol; and mineral trioxide aggregate). Data will be collected, tabulated and submitted to statistical analysis.

Conditions

  • MTA
  • Dental Restoration, Temporary

Interventions

PROCEDURE

Carie removal

Carie removal with a low speed handpiece

PROCEDURE

Relative isolation

Relative isolation with cotton and gauze.

PROCEDURE

Manipulation of the temporary material based on Zinc Oxide and Eugenol

Manipulation of the temporary material based on Zinc Oxide and Eugenol according to the manufacturer's recommendations

PROCEDURE

Manipulation of the temporary 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 cavity

Material insertion on the cavity according to the manufacturer's recommendations

PROCEDURE

Finishing the temporary direct restoration

Excess cement removal; Occlusal Adjustment; Finishing and polishing.

Sponsors & Collaborators

  • Federal University of Uberlandia

    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
2018-03-20
Primary Completion
2018-04-30
Completion
2018-10-30

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 NCT03437655 on ClinicalTrials.gov