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Sedline EEG Guided Depth of Anesthesia

NCT05051982 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 110

Last updated 2024-01-16

Study results available
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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.

Conditions

  • Anesthesia
  • Surgery

Interventions

DEVICE

Sedline EEG in View

EEG monitor (Sedline) will be in full view of the Anesthesiologist during surgery.

Sponsors & Collaborators

  • Indiana University

    lead OTHER

Principal Investigators

  • Timothy Webb, MD · Indiana University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-06-30
Primary Completion
2022-11-14
Completion
2022-11-14
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05051982 on ClinicalTrials.gov