Surgery Clinical Trial - Sedline EEG Guided Depth of Anesthesia

Status Completed

Clinical Trial Summary

The purpose of our study is to determine if monitoring sedation (how asleep patients are under general anesthesia) using a device called a Sedline Monitor affects the amount of anesthesia patients receive.

Clinical Trial Description

The main objective of this study is to determine if monitoring sedation using the FDA approved device, Sedline Monitor, affects the amount of anesthesia patients 65 or older receive during surgery. Reducing the anesthetic dose could result in less exposure of anesthetic medications to a high-risk patient population as well as a potential reduction in cost. Subjects will be randomized into either a control group or study group and have the Sedline Monitor placed on their head before the start of their already scheduled surgery. During the surgery, subjects in the control group will receive standard anesthesia care and the study group will receive anesthetic drug doses guided by Sedline Monitor processed EEG characteristics. When the surgery is complete, the Sedline Monitor will be removed and subject participation will be finished. The study team will also collect information about subjects from their medical records and use it for this study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05051982
Study type	Interventional
Source	Indiana University
Contact
Status	Completed
Phase	N/A
Start date	June 30, 2021
Completion date	November 14, 2022

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