A controlled trial of automated delivery of three intravenous anesthetics using robotic anesthesia system for total intravenous anesthesia

Not Applicable

• Conditions: Patients with ASA physical status 1-3, scheduled for surgery under total intravenous anesthesia.

• Registration Number: JPRN-jRCTs032180067
• Lead Sponsor: agata Osamu

Brief Summary

We obtained useful criteria to assess the appropriate level of analgesia that satisfies the anesthesiologist by examining in detail the information obtained from the interval when the anesthesiologists judged that the patient was in a stable analgesic state during observation period. As the non-inferiority of AC group was indicated with the revised criteria obtained in this study, our criteria will be appropriate for evaluating the effectiveness of automated-control system in future studies.

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-12-28
• Study Completion: 2019-06-30
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

1.Male and female patients over 20 years old at the time of informed consent
2.Patients with ASA physical status of 1, 2, and 3 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

Exclusion Criteria

1.Patients with a history of hypersensitive to propofol, remifentanil, rocuronium or sugammadex.
2.Patients who are pregnant or lactating.
3.Patients who are determined not to be eligible for participation in this study by the research director.

Study & Design

• Study Type: Interventional
• Study Design: Not specified