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Which cement holds Kids' crowns best? new study aims to find out

NCT ID NCT06690229

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 This study
Running, but no longer taking on new participants.
Completed
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study tests three different dental cements used to attach prefabricated zirconia crowns to children's front baby teeth. Thirty-six children with cavities will receive crowns, and researchers will check crown retention, gum health, plaque buildup, and parent satisfaction at 1 week, 3 months, 6 months, and 12 months. The goal is to find which cement works best for durability and oral health.

What this could mean

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

Active substance
dental cement (glass ionomer, self-adhesive resin, or resin modified glass ionomer)
What this could lead to
If successful, this could identify the best cement for zirconia crowns in children, improving crown retention and gum health.
What could go wrong
This is a small, early-stage trial with only 36 children, so results may not apply to all kids. It compares existing materials, not a new breakthrough.

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

About 36 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jun 2024

Expected to finish

Dec 2026

An estimate. End dates often move.

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

3 to 4 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: * Patients with consenting parents, * Patients with carious lesions on 2 or more faces of maxillary incisors or interface caries * Those whose related teeth have not undergone pulp treatment, * Patients without periodontal-related attachment loss, without tooth loss as a result of periodontal pathology, * Those requiring treatment with general anaesthesia * Score 1 and score 2 on the Frankl behaviour scale * Those without a history of allergy (such as local anaesthesia, medication, resin-based restorative materials), * Not requiring endocarditis prophylaxis, * No hypoplasia and hypomineralisation of teeth, * Patients whose permanent teeth are more than 1 year away from eruption * Patients with vital teeth and no complaints of percussion, palpation tenderness, nocturnal waking pain and no abscess and/or fistula * Teeth with a healthy lamina dura and periapical appearance * Teeth without mobility and pathological gingival pockets * Teeth with physiological root resorption not exceeding the apical 1/3 level, * No more than 2 mm alveolar bone loss in the interproximal region on the radiograph of the tooth, * No pathological internal or external root resorption, * It has a permanent tooth underneath and its position is normal, * Patients with a flush terminal closure relationship will be included in the study. Exclusion Criteria: * Teeth with periapical infection, abscess or mobility, * In cases where the depth of the gingival pocket exceeds 3 mm, * In the presence of pathological mobility, * In the presence of congenital developmental defects (amelogenesis imperfecta, dentinogenesis imperfecta), * In teeth in infraocclusion, * Patients with abnormal bite due to dental or skeletal orthodontic anomalies, * In the presence of pathological internal or external resorption, * In cases where radiographic bone loss of more than 2 mm in the interdental region is observed * Those with active periodontal disease, * Traumatised teeth, * In cases where the overjet is more than 2 mm, * Patients with deep bite * Cases where the opposite tooth is missing, * Patients with systemic diseases (diseases of the cardiovascular system, endocrine system, urinary system, central nervous system, mental disorders, etc.), * Dangerous medical conditions or harmful oral habits, * Children with bruxism or unilateral chewing habits will not be included in the study. Those who wish to withdraw from the study at any stage will be excluded from the study.

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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

  • Aydin Adnan Menderes University

    Aydin, Efeler, 09100, Turkey (Türkiye)

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Other studies related to the condition(s) this trial covers.