Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

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 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.

View on ClinicalTrials.gov ↗

View your shortlist →

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.

Interventions

  • DEVICE Intracranial Pressure Noninvasive Monitoring

Study Locations (1)

Kentucky

  • University of Louisville Health - Louisville

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2024-11-17
Est. Completion 2026-06-30

Sponsor

University of Louisville

217 total trials

What the Registry Record Tells You About NCT06511804

The ClinicalTrials.gov registry entry for NCT06511804 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 330-participant average among 22 other Brain Injuries trials with a reported enrollment target (92% lower). The listed sponsor is University of Louisville, which has 217 total studies on file at ClinicalTrials.gov.

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 1 study location spanning 1 distinct geographic area - top geographies include 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.

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.