Investigational research of an automatic control of vasoactive drug and infusion volume
- Conditions
- Patients with ASA physical status of 1 and 2, scheduled for surgery under total intravenous anesthes
- Registration Number
- JPRN-jRCTs052230120
- Lead Sponsor
- Matsuki Yuka
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
1. Male and female patients over 20 years old at the time of informed consent
2. Patients with ASA physical status of 1 and 2 who are scheduled for surgery under general anesthesia
3. Patients who understand the contents of this study and are willing to provide written informed consent for participation in this study
1. Patients with a history of hypersensitive to propofol, remifentanil, rocuronium or sugammadex
2. Patients who cannot connected BIS Sensor for placement on the forehead
3. Patients who cannot received rocuronium after first single dose
4. Patients who cannot measured non-invasive sphygmomanometer
5. Patients undergoing surgery with hypothermia
6. Patients undergoing cardiovascular surgery
7. Patients with supraventricular rhythm irregularities such as atrial fibrillation, atrial flutter, or sinus arrhythmia
8. Patients with expected blood loss of 1000 mL or more
9. Pregnant patients or patients having a possibility of pregnancy. Patients who are breast feeding or attempting to become pregnant
10. Pregnant patients or patients having a possibility of pregnancy. Patients who are breast feeding or attempting to become pregnant
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method