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Brain-Wave sedation guide cuts drug use in ventilated kids

NCT ID NCT07252024

Symptom relief Sponsor: Dr. Behcet Uz Children's Hospital 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 a special brain-wave monitor (BIS) could help nurses give the right amount of sedation to children on breathing machines in the intensive care unit. 88 children took part, and the goal was to see if using the monitor led to less time with too much or too little sedation, lower medication doses, and shorter hospital stays. The approach uses an objective brain-wave reading instead of relying only on a nurse's observation.

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

88 people

The number who actually took part.

Started

Jun 2024

Finished

Aug 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 18 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: * Age between 1 month and 18 years * Receiving invasive mechanical ventilation * Expected to require sedation for ≥24 hours * Hemodynamically stable at enrollment * BIS monitoring electrode placement feasible Exclusion Criteria: * Use of neuromuscular blocking agents at enrollment * Mechanical ventilation expected to last \<24 hours * Severe hemodynamic instability requiring escalating vasoactive support * Known neurological disorders that prevent reliable BIS interpretation (e.g., severe encephalopathy, epileptic burst suppression) * Facial burns or skin conditions preventing BIS electrode placement * Decision for palliative/comfort care only

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As listed by the trial registrant

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

Bispectral index Nurse's role Pediatric sedation

Contacts and locations

Locations

  • Behcet Uz Children's Hospital - Pediatric Intensive Care Unit

    Izmir, Turkey (Türkiye)

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