Actively Recruiting
Remimazolam Consumption: TCI vs. Manual Infusion
Led by Seoul National University Hospital · Updated on 2026-04-23
58
Participants Needed
1
Research Sites
255 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this prospective randomized controlled trial is to compare the total consumption of remimazolam between two different administration methods-Target-Controlled Infusion (TCI) and manual infusion-in patients undergoing cerebrovascular bypass surgery.
CONDITIONS
Official Title
Remimazolam Consumption: TCI vs. Manual Infusion
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients scheduled to undergo cerebrovascular bypass surgery under general anesthesia
- American Society of Anesthesiologists (ASA) Physical Status 1, 2, or 3
- Adults aged 19 years or older
- Patients who have provided prior written informed consent to participate in the study
You will not qualify if you...
- Patients who do not consent to participate in the research
- Patients classified as ASA Physical Status 4
- Patients with a BMI �3C 18.5 kg/m2 or �3E= 35.0 kg/m2
- History of allergy to benzodiazepine-class medications
- Patients with acute narrow-angle glaucoma
- Patients in a state of shock or coma
- Acute alcohol intoxication with suppressed vital signs, or patients with alcohol or drug dependency
- Presence of Sleep Apnea Syndrome or severe/acute respiratory failure
- Patients with lactose intolerance or hypersensitivity to Dextran 40
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Seoul National University Bundang Hospital
Seongnam-si, Gyeonggi-do, South Korea, 13620
Actively Recruiting
Research Team
C
Chang-Hoon Koo
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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