Passive Leg Raise and Mini-fluid Challenge Effect on Various Cardiac Output Surrogates for Fluid Responsiveness

Part of paid clinical trials in Saint Cloud, Minnesota.

Sponsor
CentraCare
Study ID
NCT06390423
Status
Recruiting

Conditions

  • Fluid Responsiveness

Eligibility Criteria

Sex
ALL
Age
30 Years - 90 Years
Healthy Volunteers
Not accepted

Interventions

  • Passive leg raise, SVI via bioreactance, Echo based VTI — DIAGNOSTIC_TEST
    No interventions other than fluid challenge

Study Details

In the critically ill population, fluid administration in an unstable patient is perhaps the most common intervention that is performed. Uncorrected hypovolemia with inappropriate vasopressors lead to organ hypoperfusion where as overzealous fluid administration especially in ARDS (Adult respiratory distress syndrome) can increase mortality. It has been estimated that only 50% of hemodynamically unstable critically ill patients are volume responsive, hence dynamic assessment of preload responsiveness has been proposed to better identify those individuals who would benefit from fluid bolus.

Key Dates

Start date
Jul 1, 2023
Status verified
Aug 2024
Primary completion
Jun 30, 2025
Completion
Jun 30, 2025

Study Design

Enrollment
64 participants (estimated)

Arms

  • Arm: Fluid responder
    Stability of vasopressor dose with maximum of 500 cc of crystalloids
  • Arm: Fluid non responder
    Escalating dose of vasopressors despite 1 L of crystalloid fluid challenge

Primary Outcome Measure

Vasopressor dose in Nor-epinephrine equivalents (NE) measured as mcg/kg/min [ Time Frame: 3 hours after the initial passive leg raise ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
St Cloud HospitalSaint CloudMinnesota56303
Ramakanth Pata, MD FCCP
320-240-2207

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