Actively Recruiting
Fuzzy Wale Compression Stockinet to Promote Healing Following Transtibial Amputation for Peripheral Arterial Disease
Led by Mayo Clinic · Updated on 2026-01-14
40
Participants Needed
1
Research Sites
77 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The objective of this study is to determine if using Fuzzy Wale compression stockinet can assist in reducing the healing time and decrease costs in transtibial amputation patients as compared to standard of care treatment compression stocking.
CONDITIONS
Official Title
Fuzzy Wale Compression Stockinet to Promote Healing Following Transtibial Amputation for Peripheral Arterial Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years
- Male and female participants
- Expected to undergo transtibial amputation
- Diagnosis of peripheral arterial disease and transcutaneous partial pressure of oxygen (if performed)
- Ability to provide informed consent or have a representative do so
You will not qualify if you...
- Known allergies to any components of the compression stockinet
- Terminal illness or current chemotherapy cancer treatment
- Inability to receive ongoing care in Rochester
- Cognitive impairment preventing following instructions or monitoring the limb
- Vulnerable study populations
- Pregnancy
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Mayo Clinic
Rochester, Minnesota, United States, 55905
Actively Recruiting
Research Team
V
Vascular Research Team
CONTACT
M
Matthew Melin, M.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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