New anesthesia combo may prevent Post-Surgery agitation
NCT ID NCT07265050
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a newer anesthesia drug (remimazolam) followed by a reversal agent (flumazenil) leads to a calmer, smoother awakening compared to standard propofol anesthesia in adults having nasal surgery. About 204 participants will be randomly assigned to one of the two methods. The main goal is to see if the new approach reduces confusion and agitation right after surgery.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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About 204 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
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.
- Ages
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19 years and older
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria \- Adults aged 19 years or older scheduled to undergo nasal surgery requiring general anesthesia Exclusion Criteria * Declines or is unable to provide informed consent * Body mass index (BMI) ≥ 30 kg/m² * Pre-existing neurological or cognitive impairment * Known contraindication or allergy to remimazolam, propofol, or flumazenil * Any condition judged by the investigator to make participation inappropriate (e.g., unstable medical status, severe comorbidities)
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Conditions
The condition(s) this trial relates to.
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 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.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a lighter sedative dose keep patients calm after nasal surgery?
- Virtual reality could replace sedatives for anxious hip surgery patients
- Can a Mother's lullaby calm children after anesthesia?
- Nose nerve block calms Post-Surgery agitation, study finds
- New study aims to calm kids after surgery with smarter anesthesia