Clinical Trials Directory

Trials / Completed

CompletedNCT03575169

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

Status
Completed
Phase
Study type
Observational
Enrollment
26 (actual)
Sponsor
University of Aberdeen · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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

Detailed description

Patients admitted to Aberdeen ICU with severe traumatic brain injury will have a BIS electrode placed and observed for 24 hours. The study team will be blinded to the result, so not to influence treatment. All clinical care is at the discretion of the clinical team.

Conditions

Interventions

TypeNameDescription
DEVICEBIS MonitorUnilateral BIS electrode

Timeline

Start date
2019-07-01
Primary completion
2022-12-31
Completion
2022-12-31
First posted
2018-07-02
Last updated
2023-01-10

Locations

4 sites across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT03575169. Inclusion in this directory is not an endorsement.

The Use of Bispectral Index Monitoring to Assess Depth of Sedation in Patients With Traumatic Brain Injury (NCT03575169) · Clinical Trials Directory