RecruitingNot Applicable

Restoration of Non-carious Cervical Lesions With Different Resin Composites and Universal Adhesive

Egypt52 participantsStarted 2022-05-14

Plain-language summary

patients with non carious cervical lesions suffer from dentin sensitivity and presence of cavitations and gingival recession. Restoring these lesions with different composites and evaluation of restorations every 6 months will be done to know the effect of different composite types and consistencies in retention of restorations of such lesions.

Who can participate

Age range

18 Years – 65 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Retention

Timeframe: 18-24 months

Trial details

NCT IDNCT06393699

SponsorAin Shams University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-12-14

Contact for this trial

Aisha Elbaz

01156686680 aishareda@dent.asu.edu.eg

View on ClinicalTrials.gov More Retention trials