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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05544903
Acronym
POCUS Sepsis
Enrollment
134
Registered
2022-09-19
Start date
2022-09-01
Completion date
2023-12-18
Last updated
2026-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sepsis

Brief 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.

Interventions

None listed

Sponsors

Northwell Health
Lead SponsorOTHER
Flosonics Medical
CollaboratorUNKNOWN

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* Already intubated prior to emergency department arrival * Ventilator-dependent * Patients transferred from another hospital * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Mortality24 hoursThis study will ascertain whether the patient died within 24 hours of ED arrival.
ICU admission24 hoursThis study will ascertain whether the patient was admitted to the ICU within 24 hours of ED arrival.
Rapid response team activation24 hoursThis study will ascertain whether a rapid response team was activated for the patient within 24 hours of ED arrival.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORAllison Cohen, MD

North Shore University Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 16, 2026