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

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, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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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.

Primary Outcome

The measure is a binary outcome: the epidural catheter is in the epidural space or not. Each modality assessed will either conclude positive (in the correct space) no negative (notnint he correct space) There is no "value". The tools used for the assessment is actually what is being studied, compuflo, meniscus test, physical exam and epidurogram.

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
University of Minnesota

966 total trials

What NCT06460155 shows while recruiting

NCT06460155 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower).

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 a single indexed study location in 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.

Similar trials for Epidural Placement

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 NCT06460155's enrollment target sits among peer trials

50 1255th of 2000 higher than 679 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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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Source: ClinicalTrials.gov NCT06460155, the US trial registry maintained by the National Library of Medicine. NCT06460155 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.