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New study seeks best pain relief for kids after hypospadias surgery

NCT ID NCT07575204

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested two types of nerve blocks to see which provides better pain relief for children aged 1 to 6 after hypospadias surgery. Sixty kids received either a pudendal nerve block or a dorsal penile nerve block, both guided by ultrasound. Researchers measured pain levels and how long relief lasted to find the safest and most effective option.

What this could mean

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

Active substance
bupivacaine and dexamethasone injection
What this could lead to
If it works, this could point toward a better way to manage pain in children after hypospadias surgery, reducing discomfort and the need for extra painkillers.
What could go wrong
This is a small, completed study with only 60 children, so results may not apply to all cases. Both techniques carry risks like allergic reactions or incomplete pain relief.

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

60 people

The number who actually took part.

Started

May 2025

Finished

Mar 2026

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

1 year to 6 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: * Patients aged 1 to 6 years. * Scheduled for hypospadias surgery under general anesthesia. * American Society of Anesthesiologists (ASA) physical status I or II (healthy children or those with mild systemic disease). * Parents or legal guardians willing to provide written informed consent. * Patients who meet the study's medical and surgical eligibility after pre-anesthetic evaluation. Exclusion Criteria: * Allergy to local anesthetics (e.g., bupivacaine). * Patient or parent refusal to participate. * Local infection or inflammation at the site of Block placement. * Anatomical deformities that may interfere with the Block administration. * Coagulopathy or bleeding disorders. * Severe systemic conditions (e.g., ASA physical status III or IV). * History of adverse reactions to nerve blocks or regional anesthesia.

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Conditions

The condition(s) this trial relates to.

hypospadias Pain, Postoperative

As listed by the trial registrant

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

Contacts and locations

Locations

  • Bangladesh Medical University

    Dhaka, 1000, Bangladesh

More trials for these conditions

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