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New study tests better fillings for kids with sensitive teeth

NCT ID NCT06987448

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study tested two types of dental overlays in 20 children aged 8-13 with Molar-Incisor Hypomineralisation (MIH), a condition that weakens enamel and causes tooth sensitivity. Each child received one overlay made from a hybrid composite and another from a hybrid ceramic, placed on opposite sides of the mouth. Over six months, dentists checked how well each material held up and whether it reduced tooth sensitivity.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
dental restoration materials (nanohybrid composite block and hybrid ceramic block)
What this could lead to
If successful, this could show which dental material works better for restoring teeth in children with MIH, leading to more comfortable and longer-lasting fillings.
What could go wrong
This is a small, short-term study (20 children, 6 months) comparing two materials. Results may not apply to all children or predict long-term performance.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

20 people

The number who actually took part.

Started

Sep 2023

Finished

Sep 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

8 to 13 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Children aged between 8 and 13 years * Presence of at least two permanent first molars affected by MIH * MIH-affected molars classified as score 2b, 2c, 4b, or 4c according to the MIH-TNI index * Symmetrical molars suitable for split-mouth comparison * Cooperative behavior sufficient to allow treatment under local anesthesia * Signed informed consent obtained from parent or legal guardian Exclusion Criteria: * Presence of systemic or syndromic diseases affecting enamel development * History of bruxism or parafunctional habits * Presence of pulp involvement, fistula, or periapical pathology in the target teeth * Allergies to dental materials used in the study (e.g., resin-based composites, adhesives) * Participation in another clinical trial within the past 30 days * Inability to attend scheduled follow-up appointments at 6, 12, and 18 months Use of medication affecting pain perception or healing process

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Marmara University, School of Dentistry, Department of Pediatric Dentistry. Marmara Üniversitesi Sağlık Yerleşkesi, Diş Hekimliği Fakültesi, Başıbüyük Yolu 9/3 34854 Başıbüyük / Maltepe / İSTANBUL.

    Istanbul, Istanbul, 34854, Turkey (Türkiye)

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