Restoring non-cavity dental lesions with different materials
Official title: 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
Run by Ain Shams University · NCT06393699 · Data updated 2026-11-12
This study is testing different materials and methods to see which works best for treating non-cavity dental lesions in patients.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 52 (estimated) |
| Sponsor | Ain Shams University Academic / other |
| Locations | 1 site (Cairo) |
| Status | Recruiting |
| Started | May 14, 2022 |
| Main results expected | December 14, 2025 |
| Study ends | December 30, 2026 |
| Registry record updated | February 27, 2025 |
| Trial ID | NCT06393699 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 to 65 with at least two non-carious cervical lesions in their premolars or canines.
✕Probably 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.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
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.
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 gone: Previous studies have shown varying success with different adhesive approaches in dental restorations, making this a relevant investigation in the field.
Who can join: the full rules
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 it's running
-
Ain shams university
Cairo, Egypt Recruiting
Study contacts
- Study coordinator: Aisha Elbaz
- Email: aishareda@dent.asu.edu.eg
- Phone: 01156686680
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.