Can the choice of anesthesia shield the aging brain after tumor surgery?
NCT ID NCT07799623
First seen Sep 02, 2026 · Last updated Sep 03, 2026 · Updated 1 time
Summary
This trial compares three common anesthetics, ciprofol, propofol, and sevoflurane, to see which one best prevents delirium, a sudden state of confusion and memory problems, in older adults after brain tumor surgery. About 381 people aged 65 to 90 will be randomly assigned to receive one of the three medicines during their operation. Researchers will track who develops delirium within 7 days after surgery, how long it lasts, and how well thinking and memory recover over 6 months. The goal is to help doctors pick the safest anesthesia for this vulnerable group.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Three anesthesia medicines: ciprofol (given intravenously), propofol (given intravenously), and sevoflurane (inhaled as a gas).
- What this could lead to
- If one anesthetic proves better at preventing delirium, doctors may choose it for older brain tumor patients to reduce confusion and protect memory after surgery.
- What could go wrong
- This is a single trial, and results may not apply to all patients. Anesthetics carry risks like blood pressure changes, and the best option may not clearly emerge.
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.
- 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 381 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 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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65 to 90 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: 1. Aged 65 to 90 years, either sex. 2. Scheduled to undergo elective brain tumor resection under general anesthesia. 3. American Society of Anesthesiologists (ASA) physical status I-III. 4. Expected operative time ≥ 2 hours and anticipated postoperative hospital stay \> 48 hours. 5. Able to communicate in Chinese and complete cognitive assessments. 6. Preoperative cognitive function intact: Telephone Montreal Cognitive Assessment (T-MoCA) score ≥ 18 and Confusion Assessment Method (CAM) negative. 7. No use of analgesic or sedative medications on the day before surgery. 8. Able to provide informed consent and willing to comply with postoperative follow-up through 180 days. Exclusion Criteria: 1. Preoperative use of medications that may affect postoperative cognition (e.g., long-term benzodiazepines, antidepressants, antipsychotics, or chronic sedative-hypnotic use that cannot be paused). 2. Preoperative delirium, dementia, diagnosed severe psychiatric disorder, or existing central nervous system disease. 3. History of alcohol addiction or drug abuse; suspected or confirmed long-term use of narcotic analgesics or sedatives. 4. Severe visual, auditory, or speech impairment that precludes communication and cognitive testing. 5. Severe cardiopulmonary disease: forced expiratory volume in 1 second (FEV1) or vital capacity \< 50% of predicted; New York Heart Association (NYHA) functional class III-IV; severe hepatic or renal insufficiency (creatinine \> 176 μmol/L, blood urea nitrogen \> 7.1 mmol/L, albumin \< 30 g/L, Child-Pugh class C, or preoperative dialysis). 6. Known difficult airway, malignant hyperthermia susceptibility, or other contraindication to general anesthesia. 7. Hypersensitivity or known allergy to ciprofol, propofol, sevoflurane, or other study-related agents. 8. Severe uncontrolled infection or endocrine disorder. 9. Concurrent participation in another clinical trial. 10. Judged unsuitable for enrollment by the attending surgeon, anesthesiologist, or principal investigator for any other reason.
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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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Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Wuhan, Hubei, 430022, China
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