New study tracks Kids' anesthesia safety with smart monitoring
NCT ID NCT07245654
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study watches how deeply children are asleep and how well their pain is controlled during the start of general anesthesia. About 100 kids aged 1 to 19 having surgery will be monitored with a special device. The goal is to see if better monitoring can prevent side effects like waking up during surgery or confusion after it.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2025
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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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
\- Pediatric patients (age 1-19 years) indicated for surgery under general anesthesia with airway management (laryngeal mask, orotracheal intubation, nasotracheal intubation) with expected duration of surgery more than 30 minutes
- Ages
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1 year to 19 years
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * Pediatric patients (age 1-19 years) indicated for surgery under general anesthesia with airway management (laryngeal mask, orotracheal intubation, nasotracheal intubation) * CONOX monitoring available Exclusion Criteria: * Age out of range * Use of ketamine during anesthesia care (premedication, analgesic, anesthetic) * Expected duration of surgery less than 30 minutes * CONOX monitoring unavailable
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University Hospital Brno
RECRUITINGBrno, 62500, Czechia
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Other studies related to the condition(s) this trial covers.
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