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Clinical Evaluation of Different Bioactive Restorative Materials for Cervical Carious in High Caries Risk Patients

NCT06736964 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2024-12-17

No results posted yet for this study

Summary

The aim of the study is to clinically evaluate three different bioactive restorative material in cervical carious lesion in high caries risk patients.

Reducing the incidence of recurrent caries is the primary outcome

Conditions

  • Class V Dental Caries
  • High Caries Risk Patients

Interventions

DEVICE

Giomer

based on Pre-reacted glass ionomer (PRG)

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Ashraf Nasr, professor · Cairo University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-10-01
Primary Completion
2026-04-01
Completion
2026-04-01
FDA Device
Yes

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 NCT06736964 on ClinicalTrials.gov