Brain Function Monitoring During Surgery

Part of paid clinical trials in Chicago, Illinois.

Sponsor
University of Chicago
Study ID
NCT06619730
Status
Recruiting
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Conditions

  • Surgery

Eligibility Criteria

Sex
ALL
Age
18 Years - 45 Years
Healthy Volunteers
Not accepted

Interventions

  • Sedline Brain Function Monitor — DEVICE
    The anesthesia provider will use the Sedline Brain Function Monitor information to affect their anesthetic dosing.

Study Details

The purpose of this research is to gather information on the effectiveness of the Sedline Brain Function Monitor, and its use in this study to determine whether monitoring the brain activity during anesthesia will improve recovery, including earlier discharge and less side effects. Furthermore, the study team wants to determine whether males and females respond to anesthetics in a similar manner with and without brain monitoring.

Key Dates

Start date
Aug 6, 2024
Status verified
Sep 2024
Primary completion
May 1, 2026
Completion
May 1, 2027

Study Design

Enrollment
100 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • No Intervention: Control Arm
    Conventional method: Anesthesia will not be guided by the Sedline brain function monitor during the procedure.
  • Active Comparator: Sedline Monitor Arm
    Anesthesia care guided by Sedline brain function monitor during the procedure.

Primary Outcome Measure

Speed of recovery time [ Time Frame: Up to 3 hours ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of Chicago Medical CenterChicagoIllinois60637
Zheng (Jimmy) Xie, MD, PhD
[email protected]
773-702-2667
Aaron Fox, PhD
[email protected]
773-702-0021

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By research site
University of Chicago Medical Center· Chicago, IL

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