Actively Recruiting
CompuFlo CathCheck
Led by University of Minnesota · Updated on 2026-01-07
50
Participants Needed
1
Research Sites
117 weeks
Total Duration
On this page
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
Eligibility Criteria
You may qualify if you...
- Adult patients aged 18 to 99 years old undergoing epidural placement for an operative procedure
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
Trial Site Locations
Total: 1 location
1
University of Minnesota
Minneapolis, Minnesota, United States, 55414
Actively Recruiting
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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