CompletedNot Applicable

Silver Diamine Fluoride Modified Restoration In Treating Hypomineralized First Permanent Molar.

Egypt42 participantsStarted 2020-09-01

Plain-language summary

A randomized clinical trial to compare silver modified glass ionomer restorations to non silver glass ionomer restorations in hypo-mineralized first permanent molars in children and to measure the amount of wear of restoration in both groups along with detecting changes in hypersensitivity in hypomineralized molars in both groups after one year follow up.

Who can participate

Age range

6 Years – 9 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: * Bilateral first permanent molars affected with molar incisor hypomineralization and with the same ICDAS II score. * Both chosen molars should be of the same degree of MIH severity. Exclusion Criteria: * signs and symptoms of irreversible pulpitis or pulp necrosis.

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

Measuring surface wear using CAD-CAM software program

Timeframe: after 1 year

Restoration Survival evaluation using the Atraumatic Restorative Treatment(ART) criteria

Timeframe: 1 year

Trial details

NCT IDNCT05931822

SponsorMansoura University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-10-30

View on ClinicalTrials.gov More Molar Incisor Hypomineralization trials