UnknownNot Applicable

Clinical Evaluation of Bioactive Restorative vs. RMGI in Class V: A Randomized Control Trial

30 participantsStarted 2019-03

Plain-language summary

Clinical performance of bioactive restorative material versus Resin Modifeid Glass Ionoer (RMGI) in class V o will be evaluated over 12 months using United State Public Health Criteria (USHPS) clinical criteria for the evaluation of direct and indirect restorations

Who can participate

Age range

18 Years – 50 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: * Cervical Class V carious lesions. * Age 18-50 years. * Co-operative patients approving to participate in the study. * Pulp asymptomatic vital carious posterior teeth. * Presence of favorable occlusion and teeth are in normal contact with the adjacent teeth. Exclusion Criteria: * Systemic disease or severe medical complications. * Allergic history concerning methacrylates * Rampant caries * Pregnancy * Disabilities * Heavy smoking; xerostomia * Lack of compliance * Evidence of severe bruxism, clenching, or temporomandibular joint disorders or bizarre habits

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

Change in the clinical performance using United State Public Health Service (USHPS)

Timeframe: Change from the baseline at 6 months and12 months

Trial details

NCT IDNCT03771196

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-08

Contact for this trial

Yehia H. Yehia

+20 01225337792 yehiahafez@dentistry.cu.edu.eg

View on ClinicalTrials.gov More Dental Restoration Failure trials

Who can participate

Age range

18 Years – 50 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.