Bispectral Monitoring on Mechanically Ventilated Patients
Recruiting
N/A
Interventional Study
Sedation
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 30 (estimated)
- Sponsor
- The University of Texas Health Science Center, Houston · Other
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About This Trial
The purpose of this study is to determine the difference in the duration of mechanical ventilation, to evaluate the difference in ICU length of stay and to determine the difference in the overall dose of sedation medications between the between participants who were monitored using Bispectral index monitoring (BIS) monitors and those who were not.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Admission to the medical ICU
* Intubated on mechanical ventilation
* On sedation medication infusion
Exclusion Criteria:
* Patients with a history of chronic opioid use
* Patients with end-stage liver disease at ICU admission (i.e., International normalized ratio \>1.5 and n…
Contacts