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New treatment option for Sedation
Official title Bispectral Monitoring on Mechanically Ventilated Patients
ClinicalTrials.gov ID: NCT07219069
What this study is testing
- What it's testing
- 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.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Admission to the medical ICU
- Intubated on mechanical ventilation
- On sedation medication infusion
You likely can't join if
- 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 not taking warfarin and/or a total serum...
- Pregnant patients
- Current prisoner
- Refractory shock: Mean arterial blood pressure below 65 millimeters of mercury(65mmHg) despite maximum doses of 3 pressors. Norepinephrine 70mcg/min...
- Inability to complete the required time for follow-up
See the full eligibility criteria
- Admission to the medical ICU
- Intubated on mechanical ventilation
- On sedation medication infusion
- 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 not taking warfarin and/or a total serum bilirubin 1.5 times above normal limits)
- Pregnant patients
- Current prisoner
- Refractory shock: Mean arterial blood pressure below 65 millimeters of mercury(65mmHg) despite maximum doses of 3 pressors. Norepinephrine 70mcg/min; vasopressin 0.03 units/min; epinephrine 35mcg/min; dopamine...
- Inability to complete the required time for follow-up
- Surgical admission diagnosis
- Patients with skin conditions precluding BIS monitor sensor adherence
- Patients on neuromuscular blockade infusion or benzodiazepine infusion
The study team makes the final eligibility decision.
Where it's taking place
- Cypress, Texas, United States
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Cypress, Texas, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.