Remimazolam Consumption: TCI vs. Manual Infusion
Recruiting now · Not applicable
Conditions studied: Moyamoya Disease
In brief
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.
Key facts
- Study ID
- NCT07377695
- Run by
- Seoul National University Hospital
- People needed
- 58
- Starts
- 2026-02-04
- Expected to finish
- 2030-12-31
- Last updated by the study team
- 2026-04-23
Who can join
Age: 19 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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 may not qualify if…
- Patients who do not consent to participate in the research
- Patients classified as ASA Physical Status 4
- Patients with a BMI ≤18.5 kg/m2 or 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
Where it is running
- Seoul National University Bundang Hospital — Seongnam-si, Gyeonggi-do, South Korea (enrolling)
Full record on ClinicalTrials.gov
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