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_TESTNo 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 responderStability of vasopressor dose with maximum of 500 cc of crystalloids
- Arm: Fluid non responderEscalating 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
- Ramakanth Pata320-240-2207
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| St Cloud Hospital | Saint Cloud | Minnesota | 56303 |