Massive study aims to end debate: which anesthetic causes less Post-Surgery confusion?
NCT ID NCT07612579
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This huge study of 100,000 adults compares two common anesthetics—propofol and sevoflurane—to see which one lowers the risk of postoperative delirium (sudden confusion after surgery). Researchers will track patients for 5 days after elective surgery. The goal is to provide clear evidence for future anesthesia guidelines and potentially reduce delirium cases in aging populations.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- propofol and sevoflurane (anesthetic drugs)
- What this could lead to
- If it works, this could show which anesthetic technique reduces delirium risk after surgery, leading to updated hospital guidelines and fewer cases of confusion in older patients.
- What could go wrong
- This is an observational study, not a controlled trial, so results may show correlation, not causation. Delirium has many causes, so even a large study may not give a clear answer.
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 100,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2026
- 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.
Who is studied
* Adult patients (≥18 years) at the Department of Anesthesiology and Intensive Care Medicine (CCM/CVK) and the Department of Anesthesiology and Intensive Care Medicine (CBF) at Charité, * undergoing elective surgery under general anesthesia * with a planned surgery duration of ≥ 30 minutes
- Ages
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18 years and older
- Sex
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Anyone
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: * Adult patients (≥18 years) at the Department of Anesthesiology and Intensive Care Medicine (CCM/CVK) and the Department of Anesthesiology and Intensive Care Medicine (CBF) at Charité, * undergoing elective surgery under general anesthesia * with a planned surgery duration of ≥ 30 minutes In addition, the following conditions must be met: * The surgery must be the patient's first surgery per hospital stay to avoid dependencies and repeated measurements of the same person within a short time frame; * The surgeries take place at Charité between January 1, 2011, and December 31, 2025. Exclusion Criteria: Patients in any of the following situations are excluded: 1. Cardiac surgery (this patient group requires specialized monitoring strategies and has postoperative delirium risk profiles that differ significantly from those of other types of surgery) 2. preoperatively diagnosed delirium, defined as positive results on the Nursing Delirium Screening Scale (NU-DESC) or the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) during preoperative evaluations; 3. severe preoperative cognitive impairment, defined as a Mini-Mental State Examination (MMSE) score \<15 points, or 4. preoperatively documented severe dementia 5. neurosurgical procedures (neurosurgical patients require specialized monitoring protocols and differ from other surgical patients in their postoperative delirium (POD) symptoms) 6. Patients who were already admitted to intensive care units prior to their elective surgery (these patients already have increased mortality and a different risk profile) 7. Patients who were already intubated or sedated prior to surgery (this group cannot undergo standardized POD screening) 8. High preoperative risk for postoperative nausea and vomiting (PONV) (specifically, patients with documented PONV grade 3 or PONV grade 4 risk are excluded, as this group is indicated for anesthesia with propofol)
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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
2 sites. 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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Department of Anesthesiology and Intensive Care Medicine (CBF), Charité - Universitätsmedizin Berlin
RECRUITINGBerlin, 12203, Germany
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Department of Anesthesiology and Intensive Care Medicine Berlin
RECRUITINGBerlin, 13353, Germany
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a common anesthetic stop Post-Surgery delirium in the elderly?
- Two sedatives, one question: can remimazolam shield the brain during aortic arch surgery?
- Can a forehead light sensor spot hidden brain oxygen drops during carotid surgery?
- Can a common sedative added to spinal anesthesia keep older minds clear after hip surgery?
- Could a sleep drug shield older hearts from post-surgery delirium?
- Could a common sedative shield aging brains from Post-Surgery delirium?