The Use of Point of Care Ultrasound to Predict Intensive Care Unit Admission of Patients Presenting With Sepsis to the Emergency Department

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The FloPatch device will be applied to 150 septic patients in the emergency department before they receive fluid resuscitation. This study will assess whether initial FloPatch measured volume-responsiveness and volume of fluids used will predict a composite outcome of mortality, intensive care unit admission, or rapid response team activation. The development of fluid unresponsiveness throughout the initial fluid resuscitation will be assessed and its association with the composite outcome will be assessed.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Emergency department patient

• 18+ years old

• Systolic blood pressure less than 100mmHg

• Respiratory rate greater than 22 breaths per minutes

• Temperature greater than 38 degrees Celsius or less than 36 degrees Celsius

• Heart rate greater than 90 beats per minute

Locations
United States
New York
North Shore University Hospital
RECRUITING
Manhasset
Contact Information
Primary
Timmy Li, PhD
tli2@northwell.edu
516-240-3933
Time Frame
Start Date: 2022-09-01
Estimated Completion Date: 2024-09
Participants
Target number of participants: 150
Treatments
Mortality, ICU admission, or rapid response team activation
Carotid flow patterns and velocity time integral values, as determined by FloPatch.
No mortality, ICU admission, or rapid response team activation
Carotid flow patterns and velocity time integral values, as determined by FloPatch.
Related Therapeutic Areas
Sponsors
Collaborators: Flosonics Medical
Leads: Northwell Health

This content was sourced from clinicaltrials.gov