A prospective study of the optimal depth of anesthesia for remimazolam anesthesia
Not Applicable
- Conditions
- ot specified
- Registration Number
- JPRN-UMIN000044418
- Lead Sponsor
- Tohoku University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Pregnant and lactating women (2) Patients with Child-Pugh classification C or higher (3) Patients with central nervous system diseases and psychiatric diseases (4) Patients who regularly use CNS-acting drugs (5) Heavy drinkers of alcohol and illegal drugs (6) Patients who cannot communicate in Japanese (7) Patients who had an adverse reaction to remimazolam and required a change in anesthetic (8) Patients who could not be awakened from anesthesia and extubated in the operating room immediately after the completion of surgery
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method EEG changes during remimazolam anesthesia
- Secondary Outcome Measures
Name Time Method The validity of a commercially available depth of anesthesia monitor