Which crown fits better for Kids' teeth? a Head-to-Head test
NCT ID NCT07738471
First seen Jul 31, 2026 · Last updated Jul 31, 2026
Summary
This trial compares two types of zirconia crowns—custom-made versus prefabricated—for restoring severely decayed baby molars after a pulpotomy (a procedure to save the tooth). Children aged 5-8 with deep cavities in their primary molars will receive one of the two crowns, and researchers will track how well each crown holds up over time, looking at fit, retention, shape, and fractures, as well as gum health. The goal is to see if custom-made crowns offer any advantage over the standard prefabricated ones, which could help dentists choose the best option for restoring young children's teeth.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Custom-made zirconia crowns or prefabricated zirconia crowns placed on pulpotomized primary molars
- What this could lead to
- If custom-made crowns perform better or equal to prefabricated ones, dentists may have a more durable and esthetic option for restoring decayed baby teeth, potentially reducing the need for re-treatment.
- What could go wrong
- This is a small, early-stage trial (64 children) comparing two dental devices, so results may not apply broadly. Crowns can fail due to poor fit, fracture, or gum irritation, and custom-made crowns may not prove superior.
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
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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
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About 64 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Nov 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2027
An estimate. End dates often move.
- Lead sponsor
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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
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5 to 8 years
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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 5-8 years. * Primary molars with deep carious lesions extending to the middle third of the dentin as confirmed radiographically. * Absence of root caries. * Absence of periapical or inter-radicular radiolucency. * Absence of internal or external root resorption. * Teeth in the opposite arch are present and in normal occlusion. * Willingness to participate and adhere to the follow-up appointments Exclusion Criteria: * Children with systemic health issues. * Children with periodontal diseases. * Children exhibiting parafunctional habits. * Uncooperative children (Frankl scale (score 1 and 2).
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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Other studies related to the condition(s) this trial covers.
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