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Compariing a Bioactive Resin Material Used As A Fissure Sealant To A Conventional Resin

NCT04052802 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2019-08-12

No results posted yet for this study

Summary

The aim of this study is to investigate the retention, marginal integrity and potential to prevent lesion progression of a bioactive resin material compared to a conventional resin-based flowable composite during management of initial carious lesion in adult population over an 18 months period.

Conditions

  • Demineralization, Tooth
  • Demineralization, Fissure
  • Non-Cavitated Caries

Interventions

OTHER

Fissure sealing

The materials will be applied to the demineralized fissures as stated in manufacturer's instructions

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-08-30
Primary Completion
2021-03-30
Completion
2021-04-30

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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 NCT04052802 on ClinicalTrials.gov