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NCT06469801 · ClinicalTrials.gov registry record · NA

ECMO ABI Detection With Hyperfine

A NA study of Stroke, Acute and Extracorporeal Membrane Oxygenation Complication, sponsored by Children's Mercy Hospital Kansas City.

Recruiting
Registry status
NA
Development phase
30
Enrollment target
1
Study location

NCT06469801 is a NA study of Stroke, Acute and Extracorporeal Membrane Oxygenation Complication that is actively recruiting participants, run by Children's Mercy Hospital Kansas City. The registered enrollment target is 30 participants, below the 629-participant average among 25 other Stroke, Acute trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06469801, a NA study of Stroke, Acute and Extracorporeal Membrane Oxygenation Complication, is actively recruiting participants, sponsored by Children's Mercy Hospital Kansas City.

RECRUITING
Registry status
NA
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

The primary objective is to characterize the prevalence and type of ABI following cannulation for pediatric patients who require ECMO support. The secondary objective is to describe the time course and rates of ABI using ultralow-field bedside MRI relative to both duration of ECMO support and clinical imaging obtained in routine care of pediatric ECMO patients.

Interventions

  • DEVICE Hyperfine

Study Locations (1)

Missouri

  • Children's Mercy - Kansas City

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2024-07-23
Est. Completion 2026-07-01
Phase NA

What the Registry Record Tells You About NCT06469801

The ClinicalTrials.gov registry entry for NCT06469801 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 629-participant average among 25 other Stroke, Acute trials with a reported enrollment target (95% lower). The listed sponsor is Children's Mercy Hospital Kansas City, which has 184 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Stroke, Acute appearing as the primary indexed condition, and to 1 intervention - of which Hyperfine is the first listed.

NCT06469801 reports 1 study location spanning 1 distinct geographic area - top geographies include Missouri.

Frequently Asked Questions

What is clinical trial NCT06469801 about?

NCT06469801 is a clinical study titled "ECMO ABI Detection With Hyperfine". The primary objective is to characterize the prevalence and type of ABI following cannulation for pediatric patients who require ECMO support. The secondary objective is to describe the time course and rates of ABI using ultralow-field bedside MRI relative to both duration of ECMO support and clinic...

What is the current status of trial NCT06469801?

This trial is currently recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2024-07-23. Estimated completion is 2026-07-01.

What conditions does trial NCT06469801 study?

This clinical trial studies the following conditions: Stroke, Acute, Extracorporeal Membrane Oxygenation Complication, Hypoxia-Ischemia, Brain, Acute Brain Injury.

What interventions are being tested in trial NCT06469801?

The interventions under investigation include: Hyperfine (DEVICE).

Who is sponsoring clinical trial NCT06469801?

This trial is sponsored by Children's Mercy Hospital Kansas City, which has 184 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06469801 being conducted?

This trial has 1 study location across Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Stroke, Acute

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

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