Evaluation of Three Different Minimally Invasive Techniques for Management of Enamel Opacities in… (NCT06135272) | Clinical Trial Compass
UnknownPhase 4
Evaluation of Three Different Minimally Invasive Techniques for Management of Enamel Opacities in Patients With Molar Incisor Hypomineralization "Randomized Controlled Clinical Trial"
Egypt75 participantsStarted 2023-12-01
Plain-language summary
The controlled clinical trial will be done to evaluate Resin infiltration, Resin modified glass ionomer varnish and Light cured giomer varnish as minimally invasive techniques for management of enamel opacities of patients with molar incisor hypomineralization. Variation in mineral density of the enamel opacity , ,Hypersensitivity, Color change of the enamel opacity, Quality of life of the patient, Parent Satisfaction will be evaluated preoperatively and at 1, 3,6,12 and 18 months of follow up.
Who can participate
Age range
6 Years – 10 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:
* Patient with molar incisor hypomineralization having at least one incisor and/or molar mildly affected.
* Patient's age ranges from 6 to 10 years old.
* The affected tooth has demarcated opacity without post eruptive enamel breakdown.
* No cavitated lesion is related to the defect or previous restorative or preventive treatment.
* The tooth is free from any symptoms of irreversible pulp inflammation.
Exclusion Criteria:
* Children who are physically or mentally disabled or having any medical condition that will affect or complicate the treatment.
* Incisors previously subjected to trauma that might lead to loss of tooth structure or compromised the pulp vitality.
* Loss of tooth structure due to 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
1
Variation in mineral density
Timeframe: It will be evaluated preoperatively and at 1, 3,6,12 and 18 months follow up.
2
Hypersensitivity
Timeframe: It will be evaluated pre operative and at 1, 3,6,12 and 18 months follow up.