Comparing different methods for securing thoracic epidural catheters

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of Dermabond as a fixation technique for thoracic epidural catheters, comparing it to two commonly used methods: Mastisol and the Grip-Lok fixation bandage. The goal is to determine which technique minimizes catheter displacement, thereby improving patient outcomes. Participants will include surgical patients aged 18 and older who are receiving a thoracic epidural. The study will exclude individuals with certain medical conditions or allergies that could affect their participation.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* surgical patient
* receiving a thoracic epidural
* 18 years of age or older

Exclusion Criteria:

* Patient refusal
* allergy to adhesives or local anesthesia
* pregnancy
* contraindication to receiving an epidural including coagulopathy, infection, elevated ICP, or severe pre-existing neurologic disorders

Where it's running

• University of Utah Health Sciences Center
  Salt Lake City, Utah, United States Recruiting

Study contacts

• Study coordinator: Ami Stuart, PhD
• Email: ami.stuart@hsc.utah.edu
• Phone: 8017934800

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.