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Dentists test two Pulp-Saving methods for Kids' deep cavities

NCT ID NCT07382115

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study compared two dental treatments for deep cavities in children's baby molars: indirect pulp treatment and direct pulp capping. Both used a special material (MTA) and a crown. Forty-five healthy children aged 7-9 took part, and the success was checked after 6 and 12 months using X-rays and exams. The goal was to see which method works better to save the tooth and avoid pain or infection.

What this could mean

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

Active substance
mineral trioxide aggregate (MTA)
What this could lead to
If successful, this could help dentists choose the best way to treat deep cavities in baby teeth, saving the tooth and avoiding more complex procedures.
What could go wrong
This is a small, completed trial with only 45 children, so results may not apply to all kids. The treatments are standard procedures, not a 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

45 people

The number who actually took part.

Started

Apr 2019

Finished

Apr 2020

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

7 to 9 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: * Systemically healthy children aged 7 to 9 years * Primary second molars with deep dentin caries indicated for vital pulp therapy * Absence of clinical signs or symptoms of irreversible pulpitis * No spontaneous or prolonged pain * Teeth with no tenderness to percussion or palpation * No pathological mobility, swelling, fistula, or abscess * Radiographic findings showing intact lamina dura and normal periodontal ligament space * Absence of periapical or furcation radiolucency * No evidence of pathological internal or external root resorption * Teeth considered restorable * Written informed consent obtained from parents Exclusion Criteria: * Children with systemic diseases or medical conditions affecting healing * Teeth with signs or symptoms of irreversible pulpitis * Presence of spontaneous pain, night pain, or prolonged pain * Teeth with periapical or furcation radiolucency * Teeth with pathological internal or external root resorption * Presence of pulpal calcifications or pulp stones * Non-restorable teeth * Lack of parental consent

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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

  • Ankara University Faculty of Dentistry

    Ankara, Ankara, Turkey (Türkiye)

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