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Characterization of Artifacts in the BIS™ EEG Signals in General Anesthesia Patients in Operating Room

NCT03553953 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 98

Last updated 2020-09-29

No results posted yet for this study

Summary

This is an observational non-invasive study which aims to collect data from patients under general anesthesia in the operating room; this data will then be used for characterization and detection of artifacts that affect the EEG signal.

Conditions

  • Anesthesia, General

Interventions

DEVICE

BIS device

Recording data from BIS device from patients who undergo elective surgery under general anesthesia

Sponsors & Collaborators

  • Medtronic - MITG

    lead INDUSTRY

Principal Investigators

  • Aeyal Raz, MD; Ph.D · Rambam Health Care Campus

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-08-15
Primary Completion
2020-08-11
Completion
2020-08-11
FDA Device
Yes

Countries

  • Israel

Study Locations

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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 NCT03553953 on ClinicalTrials.gov