Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

Which numbing method helps stop bleeding faster in Kids' Baby-Tooth procedures?

NCT ID NCT07810452

Symptom relief Sponsor: Afyonkarahisar Health Sciences University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 09, 2026 · Last updated Sep 15, 2026 · Updated 3 times

Summary

Researchers compare two ways to numb the lower jaw before a pulpotomy, a procedure that removes the top part of the pulp inside a baby molar. One method is the standard inferior alveolar nerve block given with a syringe. The other uses a computer-controlled device called QuickSleeper 5 to deliver anesthesia directly into the bone. Forty children aged 6 to 9 receive both methods in separate visits, one on each side of the mouth. The study measures how long it takes for bleeding to stop after the pulp is removed, plus pain, heart rate, and oxygen levels during treatment.

What this could mean

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

Active substance
Two local anesthesia techniques: conventional inferior alveolar nerve block and computer-controlled intraosseous anesthesia
What this could lead to
If one technique helps stop bleeding faster and causes less discomfort, dentists could choose it for pulpotomies in young children.
What could go wrong
This is a small study of 40 children at one dental school. The findings may not apply to other clinics, and the split-mouth design means each child receives both techniques, which can complicate how results are interpreted.

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 40 people

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

Started

Apr 2026

Expected to finish

Feb 2027

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

6 to 9 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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 6-9 years. * Presence of a pulpotomy indication in both mandibular primary second molars (teeth 75 and 85). * Systemically healthy children classified as ASA physical status I or II. * No known coagulation disorders. * No use of analgesic, anti-inflammatory, antithrombotic, or antipyretic medications within the previous 7 days. * Sufficient cooperation and compliance to allow completion of the planned clinical procedures. * Written informed consent obtained from a parent or legal guardian for participation in the study. * No history of a serious adverse reaction or complication associated with either of the local anesthesia techniques used in the study. Exclusion Criteria: * Children with systemic health conditions classified as ASA physical status III or higher. * Known allergy or hypersensitivity to the local anesthetic agents or other dental materials used in the study. * Presence of a known coagulation disorder or use of analgesic, anti-inflammatory, antithrombotic, or antipyretic medications within the previous 7 days. * Presence of severe infection, pulp necrosis, advanced root resorption, or any other dental condition requiring a treatment approach other than pulpotomy in the mandibular primary second molars. * Insufficient cooperation or behavioral difficulties that would prevent completion of the planned clinical procedures. * History of a serious adverse reaction or complication associated with either of the local anesthesia techniques used in the study. * Inability to comply with the study protocol or attend the scheduled study visits.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Dental caries of primary teeth are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

As listed by the trial registrant

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

Dental caries of primary teeth Pulpal bleeding; staining Pulpotomies primary teeth

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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.

Contacts and locations

Locations

  • Afyonkarahisar Health Sciences University, Faculty of Dentistry

    RECRUITING

    Afyonkarahisar, Afyonkarahisar, 03030, Turkey (Türkiye)

More trials for these conditions

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