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Nerve block eases pain and improves sleep in infants after lung surgery

NCT ID NCT06498583

Symptom relief Sponsor: Lei Xiaoming Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at whether a special nerve block (erector spinae plane block) can reduce pain and improve sleep in infants having surgery for congenital lung cysts. Sixty-eight babies were enrolled, and their pain and sleep quality were measured after surgery. The goal is to find better ways to manage pain in young children after chest surgery.

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

68 people

The number who actually took part.

Started

Jan 2024

Finished

Mar 2025

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 month to 12 months

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: * American Society of Anesthesiologists (ASA) status I-II * age 1 month - 12 mouths old * preoperative diagnosis was congenital cystic lung disease * thoracoscopic lung lesion resection(lung lobectomy or segmentectomy) Exclusion Criteria: * patient with a history of allergy to amide local anesthetics * family members refused to participate in the study. * combined congenital heart disease * patient with skin damage or infection at the proposed puncture site * patients with scoliosis

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Conditions

The condition(s) this trial relates to.

bronchogenic cyst congenital pulmonary airway malformation congenital pulmonary sequestration

As listed by the trial registrant

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

Bronchogenic cyst Bronchopulmonary sequestration Cystic adenomatoid malformation of lung, congenital

Contacts and locations

Locations

  • Second Affiliated Hospital of Xi 'an Jiaotong University

    Xi’an, Shanxi, 710004, China