Skip to main content
OpenTrials
Completed

NCT Number: NCT02833181

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Centro Hospitalar Tâmega e Sousa

Penafiel, 4564-007, Portugal

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Admitted in the ICU
  • Over 18 years old

Exclusion criteria

  • Acute neurological disease

Treatment and study plan

BIS monitor

Device

Monitoring circadian variation of EEG

Primary outcomes

  1. Circadian EEG variation

    Time frame: 24 hours

Sponsors and collaborators

Lead sponsor

Centro Hospitalar do Tâmega e Sousa

Other

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Jul 14, 2016
Registry last updated
May 23, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.