RECRUITING

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

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2022-09-01
Study Completion:2024-09
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05544903

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Emergency department patient
  2. * 18+ years old
  3. * Systolic blood pressure less than 100mmHg
  4. * Respiratory rate greater than 22 breaths per minutes
  5. * Temperature greater than 38 degrees Celsius or less than 36 degrees Celsius
  6. * Heart rate greater than 90 beats per minute
  1. * Already intubated prior to emergency department arrival
  2. * Ventilator-dependent
  3. * Patients transferred from another hospital
  4. * Pregnancy

Contacts and Locations

Study Contact

Timmy Li, PhD
CONTACT
516-240-3933
tli2@northwell.edu

Principal Investigator

Allison Cohen, MD
PRINCIPAL_INVESTIGATOR
North Shore University Hospital

Study Locations (Sites)

North Shore University Hospital
Manhasset, New York, 11030
United States

Collaborators and Investigators

Sponsor: Northwell Health

  • Allison Cohen, MD, PRINCIPAL_INVESTIGATOR, North Shore University Hospital

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-09-01
Study Completion Date2024-09

Study Record Updates

Study Start Date2022-09-01
Study Completion Date2024-09

Terms related to this study

Additional Relevant MeSH Terms

  • Sepsis