Restoring non-cavity dental lesions with different materials
Restoration of Non-carious Cervical Lesions: The Effect of Different Resin Composites Bonded With A Universal Adhesive Utilizing Two Adhesion Approaches: A Randomized Clinical Study
This study is testing different materials and methods to see which works best for treating non-cavity dental lesions in patients.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 52 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Ain Shams University Academic / other |
| Locations | 1 site (Cairo) |
| Trial ID | NCT06393699 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of various resin composites and adhesive techniques in restoring non-carious cervical lesions (NCCLs) in patients. A total of 52 participants will have two NCCLs treated on opposite sides of their mouths, using either an etch-and-rinse or self-etching adhesive approach. The restorations will be monitored for retention and performance every six months over a two-year period. The goal is to determine which combination of materials and techniques yields the best clinical outcomes.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 to 65 with at least two non-carious cervical lesions in their premolars or canines.
Not a fit: Patients with medical conditions that interfere with dental care or those with periodontal disease in the target area may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve the longevity and effectiveness of dental restorations for patients with non-carious cervical lesions.
How similar studies have performed: Previous studies have shown varying success with different adhesive approaches in dental restorations, making this a relevant investigation in the field.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: \- Patients' age will range from 18 to 65 years. * Presence of at least 2 NCCLs in one side. * Patients with no medical condition could interfere with the routine dental care. * Patients who will be able to attend for each recall visit. * Patients with healthy periodontal tissues. * Cavities presenting no more than 50% of margins in enamel. Exclusion Criteria: * Medically compromised patients. * Pregnant or breast-feeding patients. * Patients undergoing orthodontic treatment or bleaching treatment in the time of the study. * Patients with periodontal disease in the target area. * Patients presented with less than 20 teeth in the oral cavity. * Patients without antagonists. * Lesions superimposed with caries
Where this trial is running
Cairo
- Ain shams university — Cairo, Egypt (Recruiting)
Study contacts
- Study coordinator: Aisha Elbaz
- Email: aishareda@dent.asu.edu.eg
- Phone: 01156686680
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.