The Use of Bispectral Index Monitoring to Assess Depth of Sedation in Patients With Traumatic Brain Injury

NCT03575169 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 26

Last updated 2023-01-10

No results posted yet for this study

Summary

An observational study to assess the BIS reported level of sedation of patients with traumatic brain injury in the ICU.

Conditions

Interventions

DEVICE

BIS Monitor

Unilateral BIS electrode

Sponsors & Collaborators

  • NHS Grampian

    collaborator OTHER_GOV
  • University of Aberdeen

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-07-01
Primary Completion
2022-12-31
Completion
2022-12-31

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

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 NCT03575169 on ClinicalTrials.gov