Comparison of remimazolam and propofol on emergence time in patients who undergo awake craniotomy: a randomized comparative study
Not Applicable
Recruiting
- Conditions
- brain tumor
- Registration Number
- JPRN-UMIN000041353
- Lead Sponsor
- Sapporo Medical University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 126
Inclusion Criteria
Not provided
Exclusion Criteria
Patients diagnosed as severe cognitive dysfunction in preoperative period Patients who have allergy for propofol, remimazolam and flumazenil Patients who have severe hepatic dysfunction and/or renal dysfunction Patients determined as inappropriate to include by researcher of this study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method