A randomized trial of remimazolam or inhalant on postoperative quality of recovery after general anesthesia
Not Applicable
Completed
- Conditions
- Not Applicable
- Registration Number
- KCT0006288
- Lead Sponsor
- Yonsei University Wonju College of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 168
Inclusion Criteria
Patients undergoing laparoscopic cholecystectomy or gynecological robotic surgery
- between 19 years old and 65 years old
- American Society of Anesthesiologist physical status classification (ASA PS classification) = III
- estimated duration of anesthesia : 2 hours or less
Exclusion Criteria
- Ambulatory cases
- cases where a transfer is predicted to intensive care unit
- cases where intensive care is applied
- Body mass index 30 or higher
- Pregnant or breast-feeding
- Child-Turcotte-Pugh class C
- Acute narrow-angle glaumcoma
- incommunicable
- cognitive impairment
- not comprehensive to the informed consent
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method QoR-40
- Secondary Outcome Measures
Name Time Method hypotensive event;time to extubation;time to discharge to the PACU;postoperative pain in the PACU;recovery duration;administration of rescue anti-emetics