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New ultrasound technique may improve epidural success in kids

NCT ID NCT06319989

Knowledge-focused Sponsor: University of Florida Source: ClinicalTrials.gov ↗

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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 Results may not be published yet.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
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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This status has not been confirmed recently, so it may be out of date.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 tested whether using a biplane ultrasound (showing two views at once) helps doctors perform caudal epidural anesthesia more effectively in children compared to standard single-plane ultrasound. The trial involved 46 boys aged 4 months to 10 years undergoing circumcision. Researchers measured first-puncture success, procedure time, and pain relief duration to see if the biplane method offers clear advantages.

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

46 people

The number who actually took part.

Started

Aug 2024

Finished

Dec 2024

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

4 months to 10 years

Sex

Male participants only

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: * ASA I/II (Anesthesia Physical Status Classification System) * Male patients aged 4 months to 10 years * To undergo elective circumcision with caudal epidural anesthesia as an adjuvant to general anesthesia and for postoperative analgesia Exclusion Criteria: * Anatomical anomalies (e.g., tethered cord, sacral malformations, etc.). * Potential coagulopathy. * Preoperative analgesics use. * Allergy to local anesthetics. * Rash or infection at the injection site. * Female patients * Parents refuse to participate.

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As listed by the trial registrant

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

Educational problems

Contacts and locations

Locations

  • UF Health

    Gainesville, Florida, 32610, United States

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