Brain surgery delirium: can real-time monitoring protect older patients?
NCT ID NCT07797660
First seen Sep 01, 2026 · Last updated Sep 02, 2026 · Updated 1 time
Summary
This study looks at why some older adults experience delirium, a state of confusion, after brain tumor surgery. Researchers will monitor blood pressure and brain wave activity during surgery in 164 patients to see if these factors are linked to postoperative delirium. The goal is to understand the mechanisms behind this condition and find ways to prevent it.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Intraoperative monitoring of blood pressure and electroencephalogram (EEG) during brain tumor surgery
- What this could lead to
- If it works, this could lead to better ways to prevent and treat postoperative delirium in older adults after brain surgery, potentially reducing hospital stays and improving recovery.
- What could go wrong
- This is an observational study, so it cannot prove cause and effect. The findings may not apply to all patients, and the monitoring techniques may not fully capture the complex causes of delirium.
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
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About 164 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 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.
Who is studied
The study population will be selected from elderly patients scheduled to undergo elective craniotomy for intracranial tumour resection at Beijing Tiantan Hospital.
- Ages
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60 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.
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: * Patients undergoing elective craniotomy for intracranial tumour resection * Patients who will provide written informed consent Exclusion Criteria: * Patients with severe preoperative cognitive impairment precluding subsequent assessments * History of psychotropic medication use * Previous history of neurosurgical operation * Severe bradycardia (heart rate \< 40 beats per minute) * Sick-sinus syndrome or atrioventricular block of grade Ⅱ or above * Severe hepatic insufficiency (Child-Pugh grade C) * Renal failure requiring renal replacement therapy
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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 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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Beijing Tian Tan Hospital, Capital Medical University
Beijing, Beijing Municipality, 100070, China
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Other studies related to the condition(s) this trial covers.
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- A wristband that could spot delirium before it strikes?