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NCT06460155 · ClinicalTrials.gov registry record · Phase 4

CompuFlo CathCheck

A Phase 4 study of Epidural Placement, sponsored by University of Minnesota.

Recruiting
Registry status
Phase 4
Development phase
50
Enrollment target
1
Study location

NCT06460155 is a Phase 4 study of Epidural Placement that is actively recruiting participants, run by University of Minnesota. The registered enrollment target is 50 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT06460155, a Phase 4 study of Epidural Placement, is actively recruiting participants, sponsored by University of Minnesota.

RECRUITING
Registry status
Phase 4
Development phase
50 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to determine if the Compuflo CathCheck system is equivalent to an epidurogram in determining epidural catheter location (in or outside the epidural space), using the epidurogram as the gold standard. In short, this will be completed by performing an epidurogram (as is standard of practice and the gold standard of determining epidural placement) and compare it to the results of the Compuflo CathCheck system. Equivalency will be summarized through agreement and concordance. Additionally, secondary outcomes will look at how classical physical exam findings to confirm epidural placement correlate and compare to epidurogram and Compuflo CathCheck findings.

Conditions Studied

Interventions

  • DEVICE 3 methods intervention

Study Locations (1)

Minnesota

  • University of Minnesota - Minneapolis

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2024-09-30
Est. Completion 2026-12-31
Phase Phase 4

Sponsor

University of Minnesota

966 total trials

What the Registry Record Tells You About NCT06460155

The ClinicalTrials.gov registry entry for NCT06460155 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Minnesota, which has 966 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Epidural Placement appearing as the primary indexed condition, and to 1 intervention - of which 3 methods intervention is the first listed.

NCT06460155 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.

Frequently Asked Questions

What is clinical trial NCT06460155 about?

NCT06460155 is a clinical study titled "CompuFlo CathCheck". The purpose of this study is to determine if the Compuflo CathCheck system is equivalent to an epidurogram in determining epidural catheter location (in or outside the epidural space), using the epidurogram as the gold standard. In short, this will be completed by performing an epidurogram (as is st...

What is the current status of trial NCT06460155?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2024-09-30. Estimated completion is 2026-12-31.

What conditions does trial NCT06460155 study?

This clinical trial studies the following conditions: Epidural Placement.

What interventions are being tested in trial NCT06460155?

The interventions under investigation include: 3 methods intervention (DEVICE).

Who is sponsoring clinical trial NCT06460155?

This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06460155 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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