Evaluation of Circadian Variation of EEG Using BIS Monitor in ICU Patients

EEG Circadian Variation of ICU Patients Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02833181
• Other study ID #: BISEECS
• Status: Completed
• Phase: N/A
• First received: July 12, 2016
• Last updated: May 21, 2017
• Start date: July 2016
• Est. completion date: May 2017

Study information

• Verified date: May 2017
• Source: Centro Hospitalar do Tâmega e Sousa
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The investigators propose to evaluate circadian variation of EEG using BIS (bispectral index) monitor in ICU patients in three different groups: non-sedated, only sedated and sedated and curarized. BIS monitor values as SR (suppression rate), SEF (Spectral edge frequency), bispectral index and EMG (electromyography) during 24 hours in admitted patients except acute neurological disease.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: May 2017
• Est. primary completion date: April 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 100 Years

Eligibility

Inclusion Criteria:

• Admitted in the ICU

• Over 18 years old

Exclusion Criteria:

• Acute neurological disease

Related Conditions & MeSH terms

• EEG Circadian Variation of ICU Patients

Intervention

Device:
• BIS monitor
Monitoring circadian variation of EEG

Locations

Country	Name	City	State
Portugal	Centro Hospitalar Tâmega e Sousa	Penafiel

Sponsors (1)

Lead Sponsor	Collaborator
Centro Hospitalar do Tâmega e Sousa

Country where clinical trial is conducted

Portugal, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Circadian EEG variation		24 hours