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Resin Modified Glass Ionomer Versus Self-Adhesive Resin Composite Restorative Systems

NCT06543680 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 35

Last updated 2024-08-09

No results posted yet for this study

Summary

To evaluate and compare two-year clinical performance of commercially available resin modified glass ionomer cement, self-adhesive composite hybrid and self-adhesive flowable composite restorative materials for non-carious cervical lesions

Conditions

  • Secondary Caries Dental Restoration Failure of Marginal Integrity

Interventions

OTHER

Dental restoration

Each patient will randomly receive one cervical restoration with one of the tested restorative systems

Sponsors & Collaborators

  • Mansoura University

    lead OTHER

Principal Investigators

  • Mohamed E Hamouda, Assistant Lecturer · Faculty of Dentistry, Mansoura University, Egypt

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-05-29
Primary Completion
2025-05-29
Completion
2025-05-31

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 NCT06543680 on ClinicalTrials.gov