Actively Recruiting

Phase 4
Age: 18Years - 99Years
All Genders
NCT06460155

CompuFlo CathCheck

Led by University of Minnesota · Updated on 2026-01-07

50

Participants Needed

1

Research Sites

117 weeks

Total Duration

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AI-Summary

What this Trial Is About

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

Official Title

CompuFlo CathCheck

Who Can Participate

Age: 18Years - 99Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients aged 18 to 99 years old undergoing epidural placement for an operative procedure
Not Eligible

You will not qualify if you...

  • Patients unable to receive or who refuse epidural placement
  • Patients unable to give consent
  • Non-English speakers
  • Pregnant individuals
  • Individuals with a known allergy to bupivacaine

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Minnesota

Minneapolis, Minnesota, United States, 55414

Actively Recruiting

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Research Team

C

Candace Nelson

CONTACT

K

Kristine Kancans

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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