Comparing two types of dental restorative materials for non-carious cervical lesions
Resin Modified Glass Ionomer Versus Self-Adhesive Resin Composite Restorative Systems: Two Years Randomized Clinical Study in Class ᴠ
NA · Mansoura University · NCT06543680
This study is testing which of two types of dental materials works better for treating non-cavity lesions in patients' teeth over two years.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 35 (estimated) |
| Ages | 30 Years to 60 Years |
| Sex | All |
| Sponsor | Mansoura University (other) |
| Locations | 1 site (Al Mansurah, Dakahliya) |
| Trial ID | NCT06543680 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate and compare the two-year clinical performance of resin modified glass ionomer cement and two types of self-adhesive composite materials for restoring non-carious cervical lesions. The study will involve 35 patients who will each have three similarly sized lesions treated with different materials in a double-blinded, randomized design. Clinical evaluations will be conducted at baseline and throughout the study period to assess the effectiveness of each restorative material. The trial is set to take place at the Faculty of Dentistry, University of Mansoura, from May 2023 to May 2025.
Who should consider this trial
Good fit: Ideal candidates for this study are patients aged 30-60 years with at least three similarly sized non-carious cervical lesions in vital teeth.
Not a fit: Patients with severe periodontitis, mobile teeth, fractures, severe bruxism, carious teeth, poor oral hygiene, irreversible pulpitis, or endodontically treated teeth may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved dental restoration techniques, enhancing the longevity and effectiveness of treatments for patients with non-carious cervical lesions.
How similar studies have performed: While this specific comparison may be novel, similar studies evaluating restorative materials have shown varying degrees of success in improving dental restoration outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Inclusion criteria will be fair oral hygiene patients with 30-60 years. Patients with at least three similarly sized non-carious cervical lesions (NCCLs) in vital teeth that need for restoration and depth of NCCLs will be 1-3 mm with at least 50% of margins without enamel. Exclusion Criteria: * Exclusion criteria will be patients with severe periodontitis, mobile teeth, fractures, severe bruxism, carious teeth, poor oral hygiene, teeth with irreversible pulpitis and endodontically treated teeth.
Where this trial is running
Al Mansurah, Dakahliya
- Faculty of dentistry mansoura university — Al Mansurah, Dakahliya, Egypt (RECRUITING)
Study contacts
- Principal investigator: Mohamed E Hamouda, Assistant Lecturer — Faculty of Dentistry, Mansoura University, Egypt
- Study coordinator: Mohamed E Hamouda, Assistant Lecturer
- Email: mohamedelbahloul@mans.edu.eg
- Phone: 01018357630
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Secondary Caries Dental Restoration Failure of Marginal Integrity