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Brain monitor may help doctors Fine-Tune sedation during gut procedure

NCT ID NCT06866886

Knowledge-focused Sponsor: Ankara City Hospital Bilkent 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested whether a 4-channel EEG brain monitor can help doctors give the right amount of sedation during ERCP, a procedure to treat bile duct problems. 84 adults received propofol sedation, and the monitor tracked their brain activity to guide dosing. The goal was to keep patients safely sedated while allowing them to wake up quickly afterward.

What this could mean

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

Active substance
propofol
What this could lead to
If successful, this approach could help doctors tailor sedation more precisely during ERCP, potentially reducing risks and speeding up recovery.
What could go wrong
This is a small, completed study with only 84 participants. The results may not apply to all patients or settings, and the EEG monitor may not improve outcomes over standard care.

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.

Participants

84 people

The number who actually took part.

Started

Mar 2025

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.

Who is studied

Volunteer patients aged 18-65 years, of both sexes, with ASA I-II-III risk score, undergoing elective ERCP procedure

Ages

18 to 65 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: * ASA I-II-III risk score * Volunteer patients * Patients aged 18-65 years of both sexes undergoing elective ERCP procedure Exclusion Criteria: * Patient reluctance * Being under 18 years of age * Being over 65 years of age * ASA risk score of 4 and above 4 * Pregnant women * Those with neurological conditions * Patients with difficult airways * Obesity (BMI\>30)

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As listed by the trial registrant

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

Anesthesia Anesthesia, intravenous Monitoring of depth of anesthesia Recovery from anesthesia Sedation Sedation complication

Contacts and locations

Locations

  • Ankara Bilkent City Hospital

    Ankara, Turkey (Türkiye)

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