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Personalized Fluid Resuscitation in the Emergency Department: A Pilot Trial

Study acronym: FLUID-ED
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary endpoint reworded 1 of 1 changed
See other at-risk trials from Intermountain Health Care, Inc.

Record History

See every version on ClinicalTrials.gov ↗

  1. Minor Start date changed from estimate of Aug 2026 to Aug 26, 2026
    • Eligibility criteria expanded, about 31 words
    • Secondary endpoints: details revised at 3 of 6 entries
  2. Notable Primary endpoint(s) modified
    • Secondary endpoints: 4 to 6
    v2
  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this pilot clinical trial is to learn if a fluid assessment using non-invasive cardiac output monitoring (NICOM) is helpful for patients with sepsis who have low blood pressure in the Emergency Department (ED). The study will measure whether the NICOM assessment changes fluid resuscitation practices and is feasible in the ED setting. All patients will receive standard medical care. Patients assigned to the NICOM group will receive a one-time, non-invasive bedside fluid assessment using NICOM, in addition to standard care, and the results of the fluid assessment will be provided to the treating physician.
Trial Details
NCT Number NCT07779720
Lead Sponsor Intermountain Health Care, Inc.
Conditions
(from sponsor)
Sepsis, Septic Shock
Related terms Sepsis, Shock, Septic
Enrollment 40 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov