Cure My Disease

Don't miss your cure!

 Log in / Sign up

Effect of mandibular anesthesia and Computer-Controlled local anesthesia on pulp hemostasis time during pulpotomy treatment of mandibular primary molars: a Split-Mouth study

NCT ID NCT07810452

NEW 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 09, 2026

Summary

The goal of this clinical trial is to compare the effects of two local anesthesia techniques on pulp hemostasis time during pulpotomy treatment of mandibular primary molars in children aged 6-9 years. The main questions it aims to answer are: Does the local anesthesia technique affect the time required to achieve pulp hemostasis during pulpotomy? Are there differences between the two anesthesia techniques in terms of pain, heart rate, and oxygen saturation during treatment? Researchers will compare conventional inferior alveolar nerve block anesthesia with computer-controlled intraosseous local anesthesia using the QuickSleeper 5 system to determine whether the anesthesia technique affects pulp hemostasis time and the secondary clinical outcomes. Each participant will receive both anesthesia techniques in a randomized order using a split-mouth design. Participants will: Receive conventional inferior alveolar nerve block anesthesia for pulpotomy treatment of one mandibular primary molar. Receive computer-controlled intraosseous local anesthesia using the QuickSleeper 5 system for pulpotomy treatment of the contralateral mandibular primary molar at a separate treatment session. Have pulp hemostasis time recorded during each pulpotomy procedure. Have pain, heart rate, and oxygen saturation assessed during the treatment procedures.

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.

Our safety recommendation!

By submitting, you agree to our Terms of use

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

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.