Comparing different methods for securing thoracic epidural catheters
The Effects of Fixation Technique On Thoracic Epidural Catheter Displacement: A Single-Center Randomized Controlled Trial
This study tests if using Dermabond to secure thoracic epidural catheters works better than two other methods to keep them in place for surgical patients.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 300 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Utah Academic / other |
| Locations | 1 site (Salt Lake City, Utah) |
| Trial ID | NCT03976154 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates are surgical patients aged 18 and older who are scheduled to receive a thoracic epidural.
Not a fit: Patients who have allergies to adhesives, are pregnant, or have contraindications to receiving an epidural will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved fixation techniques for thoracic epidural catheters, enhancing patient safety and comfort.
How similar studies have performed: While this approach is not widely tested, similar studies on catheter fixation techniques have shown varying degrees of success.
Eligibility criteria
Show full inclusion / exclusion criteria
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 this trial is running
Salt Lake City, Utah
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.