Comparing Bond Strength,Microleakage and Clinical Performance of Three Pit and Fissure Sealants

NCT04272866 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2020-02-17

No results posted yet for this study

Summary

The aim of the study is :-

1. To evaluate and compare the microleakage of three different fissure sealants(resin-based Clinpro sealant, Moisture tolerant resin-based Embrace WetBond sealant and glass ionomer Fuji Triage sealant) in vitro.
2. To evaluate and compare the bond strength of three different fissure sealants(resin-based Clinpro sealant, Moisture tolerant resin-based Embrace WetBond sealant and glass ionomer Fuji Triage sealant) in vitro.
3. To clinically evaluate and compare the retention of three different fissure sealants(resin-based Clinpro sealant, Moisture tolerant resin-based Embrace WetBond sealant and glass ionomer-based Fuji Triage sealant).
4. To clinically evaluate and compare the caries prevention effect of three different fissure sealants(resin-based Clinpro sealant, Moisture tolerant resin-based Embrace WetBond sealant and glass ionomer-based Fuji Triage sealant).

Conditions

  • Caries Prevention

Interventions

OTHER

Clinpro sealant

Resin based sealant

OTHER

Embrace wetbond sealant

Moisture tolerant hydrophilic resin based sealant

OTHER

Triage sealant

Glass ionomer sealant

Sponsors & Collaborators

  • Sarah Emad Ali El-Din

    lead OTHER

Principal Investigators

  • Sarah E Alieldin · Faculty of dentistry ain shams university

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
FACTORIAL

Eligibility

Min Age
6 Years
Max Age
9 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-07-03
Primary Completion
2020-03-31
Completion
2020-03-31

Countries

  • Egypt

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 NCT04272866 on ClinicalTrials.gov