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Does age shape how kids wake from anesthesia?

NCT ID NCT07766629

Knowledge-focused Sponsor: Assiut University 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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 14, 2026 · Last updated Aug 14, 2026

Summary

This observational study compares how quickly and smoothly younger children (ages 3-6) recover from propofol-based intravenous anesthesia versus older children (ages 6-12). Researchers will track 64 children undergoing elective surgery, measuring the time to reach safe discharge criteria, as well as eye-opening time, pain, emergence delirium, and breathing complications. The goal is to understand how age-related differences in metabolism affect recovery, which could improve postoperative care and expectations for pediatric anesthesia.

What this could mean

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

Active substance
propofol-based total intravenous anesthesia (TIVA)
What this could lead to
If age-related recovery differences are confirmed, this could help tailor anesthesia care and discharge planning for children, improving safety and comfort after surgery.
What could go wrong
This is a small observational study, so results may not apply to all children or surgeries. It does not test a new treatment, and individual recovery can vary widely.

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

About 64 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Oct 2027

An estimate. End dates often move.

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

The study population consists of pediatric patients aged 3 to 12 years with an American Society of Anesthesiologists (ASA) physical status of I or II, scheduled for elective surgical procedures at Assiut University Hospitals. Eligible participants are those anticipated to have a surgical duration between 30 and 120 minutes and who receive propofol-based total intravenous anesthesia (TIVA) as their primary anesthetic technique. Patients are excluded from the population if they present with neurological disorders, developmental delay, hepatic or renal impairment, obesity (greater than the 95th percentile), or if they are taking concomitant sedative medications.

Ages

3 to 12 years

Sex

Anyone

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 3-12 years * ASA I-II * Elective surgery under general anaesthesia * Surgical duration 30-120 minutes * Propofol TIVA as the primary anesthetic technique Exclusion Criteria: * Neurological disorders * Developmental delay * Hepatic or renal impairment * Obesity (\>95th percentile) * Concomitant sedative medications

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Conditions

The condition(s) this trial relates to.

Emergence Delirium Postoperative Nausea and Vomiting

As listed by the trial registrant

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

Anesthesia recovery Pediatric anesthesia Total intravenous anesthesia

How to take part

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  1. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

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