Depth of Sedation and Its Impact on Cerebrovascular Reactivity in Acute Respiratory Distress Syndrome: a Pilot Analysis
Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY
Investigation of the feasibility of monitoring processed transcutaneous electroencephalography (EEG), a method of interpreting brain activity, and near-infrared spectroscopy (NIRS), a method of determining levels of tissue oxygenation (StO2) in the brain, for patients with acute respiratory distress syndrome (ARDS) in the ICU.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Adult patient admitted to the ICU
• ARDS confirmed according to the Berlin Definition
• Invasive mechanical ventilation
• Deep sedation and/or neuromuscular blockade required for ARDS treatment at the discretion of the treating medical team
• Application of monitoring devices feasible
Locations
Other Locations
Canada
Health Sciences Centre Winnipeg
RECRUITING
Winnipeg
Contact Information
Primary
Asher Mendelson, MD PhD
asher.mendelson@umanitoba.ca
204-787-8059
Time Frame
Start Date: 2024-11-25
Estimated Completion Date: 2026-01
Participants
Target number of participants: 40
Treatments
Acute Respiratory Distress Syndrome
Adults admitted to ICU with ARDS confirmed according to Berlin Definition
Related Therapeutic Areas
Sponsors
Leads: University of Manitoba