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Brain monitor may reduce Post-Surgery sickness in kids

NCT ID NCT07189845

Symptom relief Sponsor: Engin Çetin Source: ClinicalTrials.gov ↗

What the study statuses mean

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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 Results may not be published yet.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
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This status has not been confirmed recently, so it may be out of date.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 using a brain activity monitor (BIS) during anesthesia can lower the chance of nausea and vomiting after surgery in children aged 3 to 8. Fifty-eight children having their tonsils removed took part. Half received standard anesthesia care, and the other half had anesthesia guided by the BIS monitor. The goal was to see if the monitor helped reduce sickness in the first 24 hours after 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

58 people

The number who actually took part.

Started

Sep 2025

Finished

Jan 2026

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

3 to 8 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: * Children aged 3-8 years * ASA physical status class I-II * Scheduled for elective adenoidectomy * Written informed consent obtained from parents Exclusion Criteria: * Children with a previous history of PONV * Patients receiving antiemetic, steroid, or sedative medication * Acute upper respiratory tract infection * History of neurological or psychiatric disorders * Body mass index (BMI) below the 5th percentile or above the 95th percentile * Anatomical airway abnormalities

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Conditions

The condition(s) this trial relates to.

Postoperative Nausea and Vomiting

As listed by the trial registrant

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

BIS PONV

Contacts and locations

Locations

  • University of Health Sciences Kocaeli City Hospital

    Kocaeli, Izmit, 41100, Turkey (Türkiye)

More trials for these conditions

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