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NCT06511804 · ClinicalTrials.gov registry record
Correlation Between Noninvasive Blood Vessel Functionality Parameters and Cerebral Hemodynamics in Neurocritical Care Patients
A clinical trial of Brain Injuries and Intracranial Pressure Increase, sponsored by University of Louisville.
- Recruiting
- Registry status
- 25
- Enrollment target
- 1
- Study location
NCT06511804: Recruiting study of Brain Injuries and Intracranial Pressure Increase, sponsored by University of Louisville.
NCT06511804 is a study of Brain Injuries and Intracranial Pressure Increase that is actively recruiting participants, run by University of Louisville. The registered enrollment target is 25 participants, below the 330-participant average among 22 other Brain Injuries trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06511804, a study of Brain Injuries and Intracranial Pressure Increase, is actively recruiting participants, sponsored by University of Louisville.
- RECRUITING
- Registry status
- 25 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this clinical research project is to employ Mespere LifeSciences NeurOs Cerebral Oximetry system, equipped with noninvasive sensors approved by the FDA, to monitor and investigate the correlation within a cohort of patients suffering from traumatic brain injury (TBI), stroke, brain tumor, and brain bleeding. This study aims to investigate and establish the correlation between blood vessel functionality parameters-specifically, Vasodilation/Constriction Index (VDC), Vascular Resistance Index (VR), and Volume Reactivity Index (VRx)-with the crucial physiological indicators, Intracranial Pressure (ICP) and Mean Arterial Pressure (MAP). By doing so, the investigators seek to address fundamental questions surrounding cerebral hemodynamics and autoregulation in various neurological conditions.
Primary Outcome
cerebral hemodynamics and autoregulation as assessed by the noninvasive blood vessel functionality parameters-Vasodilation/Constriction Index (VDC), Vascular Resistance Index (VR), and Volume Reactivity Index (VRx)-in patients with traumatic brain injury, stroke, brain bleeding
Conditions Studied
Interventions
- DEVICE Intracranial Pressure Noninvasive Monitoring
Study Locations (1)
Kentucky
- University of Louisville Health - Louisville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 25 participants |
| Start Date | 2024-11-17 |
| Est. Completion | 2026-06-30 |
What NCT06511804 shows while recruiting
NCT06511804 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 330-participant average among 22 other Brain Injuries trials with a reported enrollment target (92% lower).
The record links to 3 conditions, with Brain Injuries appearing as the primary indexed condition, and to 1 intervention - of which Intracranial Pressure Noninvasive Monitoring is the first listed.
NCT06511804 reports a single indexed study location in Kentucky.
Frequently Asked Questions
What is clinical trial NCT06511804 about?
NCT06511804 is a clinical study titled "Correlation Between Noninvasive Blood Vessel Functionality Parameters and Cerebral Hemodynamics in Neurocritical Care Patients". The purpose of this clinical research project is to employ Mespere LifeSciences NeurOs Cerebral Oximetry system, equipped with noninvasive sensors approved by the FDA, to monitor and investigate the correlation within a cohort of patients suffering from traumatic brain injury (TBI), stroke, brain tu...
What is the current status of trial NCT06511804?
This trial is currently recruiting. The enrollment target is 25 participants. The study started on 2024-11-17. Estimated completion is 2026-06-30.
What conditions does trial NCT06511804 study?
This clinical trial studies the following conditions: Brain Injuries, Intracranial Pressure Increase, Monitoring.
What interventions are being tested in trial NCT06511804?
The interventions under investigation include: Intracranial Pressure Noninvasive Monitoring (DEVICE).
Who is sponsoring clinical trial NCT06511804?
This trial is sponsored by University of Louisville, which has 217 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06511804 being conducted?
This trial has 1 study location across Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Brain Injuries
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06511804's enrollment target sits among peer trials
25 22nd of 22 higher than 1 of 22 other Brain Injuries trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Brain Injuries trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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