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NCT06390423 · ClinicalTrials.gov registry record
Passive Leg Raise and Mini-fluid Challenge Effect on Various Cardiac Output Surrogates for Fluid Responsiveness
A clinical trial of Fluid Responsiveness, sponsored by CentraCare.
- Recruiting
- Registry status
- 64
- Enrollment target
- 1
- Study location
NCT06390423 is a study of Fluid Responsiveness that is actively recruiting participants, run by CentraCare. The registered enrollment target is 64 participants. The trial reports 1 study location across 1 state.
The verdict
NCT06390423, a study of Fluid Responsiveness, is actively recruiting participants, sponsored by CentraCare.
- RECRUITING
- Registry status
- 64 participants
- Enrollment target
- 1
- Study location
Study Summary
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.
Conditions Studied
Interventions
- DIAGNOSTIC_TEST Passive leg raise, SVI via bioreactance, Echo based VTI
Study Locations (1)
Minnesota
- St Cloud Hospital - Saint Cloud
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 64 participants |
| Start Date | 2023-07-01 |
| Est. Completion | 2025-06 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06390423
The ClinicalTrials.gov registry entry for NCT06390423 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 64 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is CentraCare, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Fluid Responsiveness appearing as the primary indexed condition, and to 1 intervention - of which Passive leg raise, SVI via bioreactance, Echo based VTI is the first listed.
NCT06390423 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.
Frequently Asked Questions
What is clinical trial NCT06390423 about?
NCT06390423 is a clinical study titled "Passive Leg Raise and Mini-fluid Challenge Effect on Various Cardiac Output Surrogates for Fluid Responsiveness". 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...
What is the current status of trial NCT06390423?
This trial is currently recruiting. The enrollment target is 64 participants. The study started on 2023-07-01. Estimated completion is 2025-06.
What conditions does trial NCT06390423 study?
This clinical trial studies the following conditions: Fluid Responsiveness.
What interventions are being tested in trial NCT06390423?
The interventions under investigation include: Passive leg raise, SVI via bioreactance, Echo based VTI (DIAGNOSTIC_TEST).
Who is sponsoring clinical trial NCT06390423?
This trial is sponsored by CentraCare, which has 3 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06390423 being conducted?
This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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